A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509546



Internal ID18807827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15884287..15965916hg38UCSC Ensembl
Innerchr10:15926286..16007915hg19UCSC Ensembl
Innerchr10:15966292..16047921hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3881630
hg1981630
hg1881630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039793
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)nssv3509546
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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