A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705203



Internal ID15441855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:126004923..126018389hg38UCSC Ensembl
Innerchr5:125340616..125354082hg19UCSC Ensembl
Innerchr5:125368515..125381981hg18UCSC Ensembl
Innerchr5:125368515..125381981hg17UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3813467
hg1913467
hg1813467
hg1713467
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528582
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705203
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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