A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594743



Internal ID16035466
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 StatusM
Merged Variants
Supporting Variantsnssv1002612
Samples
Known GenesHNRNPD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594743
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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