A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595826



Internal ID16383235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160118192..160158193hg38UCSC Ensembl
Innerchr4:161039344..161079345hg19UCSC Ensembl
Innerchr4:161258794..161298795hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3840002
hg1940002
hg1840002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9334n54
Supporting Variantsnssv1009798, nssv1009799
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595826
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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