A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520053



Internal ID18818334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56970885..57122072hg38UCSC Ensembl
Innerchr10:58730645..58881832hg19UCSC Ensembl
Innerchr10:58400651..58551838hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38151188
hg19151188
hg18151188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053600
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)nssv3520053
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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