A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576377



Internal ID16363786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5324787..5337439hg38UCSC Ensembl
Innerchr18:5324786..5337438hg19UCSC Ensembl
Innerchr18:5314786..5327438hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3812653
hg1912653
hg1812653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877898
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576377
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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