A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669567



Internal ID15059533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:88673046..88708284hg38UCSC Ensembl
Innerchr5:87968864..88004101hg19UCSC Ensembl
Innerchr5:88004620..88039857hg18UCSC Ensembl
Innerchr5:88004620..88039857hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3835239
hg1935238
hg1835238
hg1735238
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515977
Supporting Variants
Samples
Known GenesLINC00461
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669567
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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