A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701227



Internal ID15437879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:13810829..13819674hg38UCSC Ensembl
Innerchr18:13810828..13819673hg19UCSC Ensembl
Innerchr18:13800828..13809673hg18UCSC Ensembl
Innerchr18:13800828..13809673hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg388846
hg198846
hg188846
hg178846
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525155
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701227
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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