A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693024



Internal ID15082990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5297563..5335470hg38UCSC Ensembl
Innerchr9:5297563..5335470hg19UCSC Ensembl
Innerchr9:5287563..5325470hg18UCSC Ensembl
Innerchr9:5287563..5325470hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3837908
hg1937908
hg1837908
hg1737908
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516752
Supporting Variants
Samples
Known GenesRLN1, RLN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693024
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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