A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599821



Internal ID18898102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19586878..20152158hg38UCSC Ensembl
Innerchr21:20959192..21524471hg19UCSC Ensembl
Innerchr21:19881063..20446342hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38565281
hg19565280
hg18565280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063624
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)nssv3599821
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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