A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593617



Internal ID16381026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7570991..7618468hg38UCSC Ensembl
Innerchr4:7572718..7620195hg19UCSC Ensembl
Innerchr4:7623618..7671095hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3847478
hg1947478
hg1847478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv991222
Samples
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593617
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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