A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685487



Internal ID15075453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:56771299..56815915hg38UCSC Ensembl
Innerchr18:54438530..54483146hg19UCSC Ensembl
Innerchr18:52589528..52634144hg18UCSC Ensembl
Innerchr18:52589528..52634144hg17UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3844617
hg1944617
hg1844617
hg1744617
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)nssv685487
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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