A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002632



Internal ID15949902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:85650459..85651480hg38UCSC Ensembl
Innerchr4:86571612..86572633hg19UCSC Ensembl
Innerchr4:86790636..86791657hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg381022
hg191022
hg181022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594755
Supporting Variants
Samples
Known GenesARHGAP24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002632
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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