A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524112



Internal ID15451405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:35760285..35777904hg38UCSC Ensembl
Innerchr18:33340249..33357868hg19UCSC Ensembl
Innerchr18:31594247..31611866hg18UCSC Ensembl
Innerchr18:31594247..31611866hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3817620
hg1917620
hg1817620
hg1717620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699990
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524112
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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