A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599830



Internal ID18898111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:20202324..20276862hg38UCSC Ensembl
Innerchr21:21574637..21649174hg19UCSC Ensembl
Innerchr21:20496508..20571045hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3874539
hg1974538
hg1874538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060546
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)nssv3599830
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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