A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504206



Internal ID18802487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19126646..19543118hg38UCSC Ensembl
Innerchr10:19415575..19832047hg19UCSC Ensembl
Innerchr10:19455581..19872053hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38416473
hg19416473
hg18416473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035870
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)nssv3504206
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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