A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3495025



Internal ID19082666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11395684..11419383hg38UCSC Ensembl
Innerchr10:11437683..11461382hg19UCSC Ensembl
Innerchr10:11477689..11501388hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3823700
hg1923700
hg1823700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054091
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)nssv3495025
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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