A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3500944



Internal ID19088585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623495..5683245hg38UCSC Ensembl
Innerchr10:5665458..5725208hg19UCSC Ensembl
Innerchr10:5705464..5765214hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3859751
hg1959751
hg1859751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049620
Supporting Variants
Samples
Known GenesASB13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3500944
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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