A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576595



Internal ID16364004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29480465..29556114hg38UCSC Ensembl
Innerchr18:27060430..27136079hg19UCSC Ensembl
Innerchr18:25314428..25390077hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3875650
hg1975650
hg1875650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878870
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576595
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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