A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693099



Internal ID15429751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:30235355..30235644hg38UCSC Ensembl
Innerchr18:27815320..27815609hg19UCSC Ensembl
Innerchr18:26069318..26069607hg18UCSC Ensembl
Innerchr18:26069318..26069607hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38290
hg19290
hg18290
hg17290
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516109
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693099
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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