A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683803



Internal ID15073769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:56773966..56898124hg38UCSC Ensembl
Innerchr18:54441197..54565355hg19UCSC Ensembl
Innerchr18:52592195..52716353hg18UCSC Ensembl
Innerchr18:52592195..52716353hg17UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38124159
hg19124159
hg18124159
hg17124159
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517361
Supporting Variants
Samples
Known GenesWDR7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683803
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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