A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662642



Internal ID15052608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:907520..910634hg38UCSC Ensembl
Innerchr18:907521..910635hg19UCSC Ensembl
Innerchr18:897521..900635hg18UCSC Ensembl
Innerchr18:897521..900635hg17UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg383115
hg193115
hg183115
hg173115
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)nssv662642
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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