A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596364



Internal ID16383773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184846022..184847547hg38UCSC Ensembl
Innerchr4:185767176..185768701hg19UCSC Ensembl
Innerchr4:186004170..186005695hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381526
hg191526
hg181526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9421n54
Supporting Variantsnssv1017973
Samples
Known GenesLOC731424
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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