A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv467634



Internal ID15035594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:50064122..50065995hg38UCSC Ensembl
Outerchr12:50060574..50068355hg38UCSC Ensembl
Innerchr12:50457905..50459778hg19UCSC Ensembl
Outerchr12:50454357..50462138hg19UCSC Ensembl
Innerchr12:48744172..48746045hg18UCSC Ensembl
Outerchr12:48740624..48748405hg18UCSC Ensembl
Innerchr12:48744172..48746045hg16UCSC Ensembl
Outerchr12:48740624..48748405hg16UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg387782
hg197782
hg187782
hg167782
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele OriginGermline
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv437753
Supporting Variants
SamplesNA19208
Known GenesASIC1
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nssv467634
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer