A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596362



Internal ID16383771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184846022..184847115hg38UCSC Ensembl
Innerchr4:185767176..185768269hg19UCSC Ensembl
Innerchr4:186004170..186005263hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381094
hg191094
hg181094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9421n54
Supporting Variantsnssv1017970
Samples
Known GenesLOC731424
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596362
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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