A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697859



Internal ID15434511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8724459..8737476hg38UCSC Ensembl
Innerchr18:8724457..8737474hg19UCSC Ensembl
Innerchr18:8714457..8727474hg18UCSC Ensembl
Innerchr18:8714457..8727474hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3813018
hg1913018
hg1813018
hg1713018
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521231
Supporting Variants
Samples
Known GenesSOGA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697859
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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