A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594691



Internal ID16035414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:76040649..76051441hg38UCSC Ensembl
Innerchr4:76961802..76972594hg19UCSC Ensembl
Innerchr4:77180826..77191618hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3810793
hg1910793
hg1810793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9135n54
Supporting Variantsnssv1002367
Samples
Known GenesART3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594691
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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