A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576596



Internal ID16364005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29578360..29726860hg38UCSC Ensembl
Innerchr18:27158325..27306825hg19UCSC Ensembl
Innerchr18:25412323..25560823hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38148501
hg19148501
hg18148501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878871
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576596
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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