A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665275



Internal ID15401927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:53196847..53250011hg38UCSC Ensembl
Innerchr5:52492677..52545841hg19UCSC Ensembl
Innerchr5:52528434..52581598hg18UCSC Ensembl
Innerchr5:52528434..52581598hg17UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3853165
hg1953165
hg1853165
hg1753165
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515913
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665275
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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