A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520160



Internal ID15100767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:54836082..54836358hg38UCSC Ensembl
Innerchr18:52503313..52503589hg19UCSC Ensembl
Innerchr18:50654311..50654587hg18UCSC Ensembl
Innerchr18:50654311..50654587hg17UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38277
hg19277
hg18277
hg17277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662015, nssv671775, nssv661295, nssv680144, nssv683892
Samples
Known GenesRAB27B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520160
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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