A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583662



Internal ID18881943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10512710..10775598hg38UCSC Ensembl
Innerchr21:10736859..10999747hg19UCSC Ensembl
Innerchr21:9758730..10021618hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38262889
hg19262889
hg18262889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066007
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)nssv3583662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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