A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv995931



Internal ID16289887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39044710..39045265hg38UCSC Ensembl
Innerchr4:39046330..39046885hg19UCSC Ensembl
Innerchr4:38722725..38723280hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38556
hg19556
hg18556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594013
Supporting Variants
Samples
Known GenesKLHL5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv995931
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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