A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653629



Internal ID15043595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:65696393..65709378hg38UCSC Ensembl
Innerchr5:64992220..65005205hg19UCSC Ensembl
Innerchr5:65027976..65040961hg18UCSC Ensembl
Innerchr5:65027976..65040961hg17UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3812986
hg1912986
hg1812986
hg1712986
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517021
Supporting Variants
Samples
Known GenesSGTB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653629
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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