A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037490



Internal ID18780021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46267036hg38UCSC Ensembl
Innerchr10:47541177..47638272hg19UCSC Ensembl
Innerchr10:47011183..47108278hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3897096
hg1997096
hg1897096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv830n100
Supporting Variantsnssv3505043
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037490
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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