A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732530



Internal ID19030811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10550046..10753328hg38UCSC Ensembl
Innerchr21:10759129..10962411hg19UCSC Ensembl
Innerchr21:9781000..9984282hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38203283
hg19203283
hg18203283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059412
Supporting Variants
Samples
Known GenesTPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3732530
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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