A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521374



Internal ID18819655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81488191..81591486hg38UCSC Ensembl
Innerchr10:83247947..83351242hg19UCSC Ensembl
Innerchr10:83237927..83341222hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38103296
hg19103296
hg18103296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043757
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)nssv3521374
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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