A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152405



Internal ID15873423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38744120..38785200hg38UCSC Ensembl
Innerchr21:40116044..40157124hg19UCSC Ensembl
Innerchr21:39037914..39078994hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3841081
hg1941081
hg1841081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587476
Supporting Variants
SamplesHGDP00197
Known GenesLINC00114
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152405
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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