A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv948404



Internal ID15895674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44523723..44524882hg38UCSC Ensembl
Innerchr21:45943606..45944765hg19UCSC Ensembl
Innerchr21:44768034..44769193hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381160
hg191160
hg181160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587808
Supporting Variants
Samples
Known GenesTSPEAR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv948404
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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