A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664758



Internal ID15054724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:56757644..56870161hg38UCSC Ensembl
Innerchr18:54424875..54537392hg19UCSC Ensembl
Innerchr18:52575873..52688390hg18UCSC Ensembl
Innerchr18:52575873..52688390hg17UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38112518
hg19112518
hg18112518
hg17112518
Variant TypeCNV gain
Copy Number
Allele State
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)nssv664758
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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