A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514229



Internal ID18812510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56575142..56725241hg38UCSC Ensembl
Innerchr10:58334902..58485001hg19UCSC Ensembl
Innerchr10:58004908..58155007hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38150100
hg19150100
hg18150100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047726
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)nssv3514229
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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