A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576644



Internal ID16364053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:33803925..33837208hg38UCSC Ensembl
Innerchr18:31383889..31417172hg19UCSC Ensembl
Innerchr18:29637887..29671170hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3833284
hg1933284
hg1833284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5884n54
Supporting Variantsnssv1149713
Samples1780862276_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576644
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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