A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3496380



Internal ID18737335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1136183..1472931hg38UCSC Ensembl
Innerchr10:1182123..1515126hg19UCSC Ensembl
Innerchr10:1172123..1505126hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38336749
hg19333004
hg18333004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047911
Supporting Variants
Samples
Known GenesADARB2, LINC00200
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3496380
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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