A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697978



Internal ID15087944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:24468583..24479130hg38UCSC Ensembl
Innerchr18:22048547..22059094hg19UCSC Ensembl
Innerchr18:20302545..20313092hg18UCSC Ensembl
Innerchr18:20302545..20313092hg17UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3810548
hg1910548
hg1810548
hg1710548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521369
Supporting Variants
Samples
Known GenesHRH4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697978
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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