A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700773



Internal ID15090739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:129575356..129724532hg38UCSC Ensembl
Innerchr6:129896501..130045677hg19UCSC Ensembl
Innerchr6:129938194..130087370hg18UCSC Ensembl
Innerchr6:129938194..130087370hg17UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38149177
hg19149177
hg18149177
hg17149177
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524782
Supporting Variants
Samples
Known GenesARHGAP18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700773
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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