A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593346



Internal ID16034069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1870601..1891901hg38UCSC Ensembl
Innerchr4:1872328..1893628hg19UCSC Ensembl
Innerchr4:1842126..1863426hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3821301
hg1921301
hg1821301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv988460
Samples
Known GenesWHSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593346
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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