A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682031



Internal ID15071997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:147201162..147212003hg38UCSC Ensembl
Innerchr5:146580725..146591566hg19UCSC Ensembl
Innerchr5:146560918..146571759hg18UCSC Ensembl
Innerchr5:146560918..146571759hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3810842
hg1910842
hg1810842
hg1710842
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519847
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682031
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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