A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699995



Internal ID15436647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18676765..18738188hg38UCSC Ensembl
Innerchr5:18676874..18738297hg19UCSC Ensembl
Innerchr5:18712631..18774054hg18UCSC Ensembl
Innerchr5:18712631..18774054hg17UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3861424
hg1961424
hg1861424
hg1761424
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524117
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699995
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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