A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705599



Internal ID15442251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6695652..6699111hg38UCSC Ensembl
Innerchr5:6695765..6699224hg19UCSC Ensembl
Innerchr5:6748765..6752224hg18UCSC Ensembl
Innerchr5:6748765..6752224hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg383460
hg193460
hg183460
hg173460
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515717
Supporting Variants
Samples
Known GenesLOC100505625
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705599
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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