A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002612



Internal ID15949882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:82353481..82404421hg38UCSC Ensembl
Innerchr4:83274634..83325574hg19UCSC Ensembl
Innerchr4:83493658..83544598hg18UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3850941
hg1950941
hg1850941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594743
Supporting Variants
Samples
Known GenesHNRNPD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002612
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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