A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600122



Internal ID18898403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32037619..32098317hg38UCSC Ensembl
Innerchr21:33409932..33470630hg19UCSC Ensembl
Innerchr21:32331803..32392501hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3860699
hg1960699
hg1860699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056554
Supporting Variants
Samples
Known GenesLINC00159
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600122
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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