A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576544



Internal ID16363953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15045812..15209635hg38UCSC Ensembl
Innerchr18:15045811..15209634hg19UCSC Ensembl
Innerchr18:15035811..15199634hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38163824
hg19163824
hg18163824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5868n54
Supporting Variantsnssv878462
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576544
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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