A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656211



Internal ID15046177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:907520..907709hg38UCSC Ensembl
Innerchr18:907521..907710hg19UCSC Ensembl
Innerchr18:897521..897710hg18UCSC Ensembl
Innerchr18:897521..897710hg17UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38190
hg19190
hg18190
hg17190
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517252
Supporting Variants
Samples
Known GenesADCYAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656211
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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