A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3492439



Internal ID19080080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9897694..9988666hg38UCSC Ensembl
Innerchr10:9939657..10030629hg19UCSC Ensembl
Innerchr10:9979663..10070635hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3890973
hg1990973
hg1890973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047670
Supporting Variants
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)nssv3492439
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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