A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674181



Internal ID15410833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:72460275..72460843hg38UCSC Ensembl
Innerchr5:71756102..71756670hg19UCSC Ensembl
Innerchr5:71791858..71792426hg18UCSC Ensembl
Innerchr5:71791858..71792426hg17UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38569
hg19569
hg18569
hg17569
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516808
Supporting Variants
Samples
Known GenesZNF366
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674181
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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