A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669284



Internal ID15405936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152135395..152148270hg38UCSC Ensembl
Innerchr5:151514956..151527831hg19UCSC Ensembl
Innerchr5:151495149..151508024hg18UCSC Ensembl
Innerchr5:151495149..151508024hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3812876
hg1912876
hg1812876
hg1712876
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516251
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669284
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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