A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707672



Internal ID18659267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4874422..4932389hg38UCSC Ensembl
Innerchr10:4916614..4974581hg19UCSC Ensembl
Innerchr10:4906614..4964581hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3857968
hg1957968
hg1857968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042940
Supporting Variants
Samples
Known GenesAKR1C6P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707672
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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