A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599887



Internal ID18898168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:22077666..22241687hg38UCSC Ensembl
Innerchr21:23449985..23614007hg19UCSC Ensembl
Innerchr21:22371856..22535878hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38164022
hg19164023
hg18164023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063589
Supporting Variants
Samples
Known GenesLINC00308
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3599887
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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