A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039682



Internal ID19128901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63688137..63781223hg38UCSC Ensembl
Innerchr13:64262270..64355356hg19UCSC Ensembl
Innerchr13:63160271..63253357hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3893087
hg1993087
hg1893087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1686n100
Supporting Variantsnssv3526617
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039682
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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