A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599979



Internal ID18898260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:23040548..23202607hg38UCSC Ensembl
Innerchr21:24412870..24574929hg19UCSC Ensembl
Innerchr21:23334741..23496800hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38162060
hg19162060
hg18162060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058500
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)nssv3599979
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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