A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658391



Internal ID15395043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:149598542..149627163hg38UCSC Ensembl
Innerchr5:148978105..149006726hg19UCSC Ensembl
Innerchr5:148958298..148986919hg18UCSC Ensembl
Innerchr5:148958298..148986919hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3828622
hg1928622
hg1828622
hg1728622
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516760
Supporting Variants
Samples
Known GenesARHGEF37
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658391
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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