A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519069



Internal ID18817350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70625308..70665972hg38UCSC Ensembl
Innerchr10:72385064..72425728hg19UCSC Ensembl
Innerchr10:72055070..72095734hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3840665
hg1940665
hg1840665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052240
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)nssv3519069
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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