A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv467017



Internal ID15381558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:6134450..6137280hg38UCSC Ensembl
Outerchr12:6129313..6154653hg38UCSC Ensembl
Innerchr12:6243616..6246446hg19UCSC Ensembl
Outerchr12:6238479..6263819hg19UCSC Ensembl
Innerchr12:6113877..6116707hg18UCSC Ensembl
Outerchr12:6108740..6134080hg18UCSC Ensembl
Innerchr12:6113877..6116707hg16UCSC Ensembl
Outerchr12:6108740..6134080hg16UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3825341
hg1925341
hg1825341
hg1625341
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele OriginGermline
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv437136
Supporting Variants
SamplesNA10851
Known Genes
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)nssv467017
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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