A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037762



Internal ID19126981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105345043..105534397hg38UCSC Ensembl
Innerchr10:107104801..107294155hg19UCSC Ensembl
Innerchr10:107094791..107284145hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38189355
hg19189355
hg18189355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv968n100
Supporting Variantsnssv3504277
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037762
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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