A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697042



Internal ID15433694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8566681..8582181hg38UCSC Ensembl
Innerchr18:8566679..8582179hg19UCSC Ensembl
Innerchr18:8556679..8572179hg18UCSC Ensembl
Innerchr18:8556679..8572179hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3815501
hg1915501
hg1815501
hg1715501
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519772
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697042
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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