A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437317



Internal ID15036049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:991423..995193hg38UCSC Ensembl
Outerchr3:988744..998855hg38UCSC Ensembl
Innerchr3:1033107..1036877hg19UCSC Ensembl
Outerchr3:1030428..1040539hg19UCSC Ensembl
Innerchr3:1008107..1011877hg18UCSC Ensembl
Outerchr3:1005428..1015539hg18UCSC Ensembl
Innerchr3:1008107..1011877hg16UCSC Ensembl
Outerchr3:1005428..1015539hg16UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3810112
hg1910112
hg1810112
hg1610112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467198
SamplesNA18500
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)nsv437317
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