A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576670



Internal ID16364079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39362493..39509651hg38UCSC Ensembl
Innerchr18:36942457..37089615hg19UCSC Ensembl
Innerchr18:35196455..35343613hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38147159
hg19147159
hg18147159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv879926
Samples
Known GenesLINC00669
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576670
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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