A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576649



Internal ID16364058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:34114603..34247871hg38UCSC Ensembl
Innerchr18:31694567..31827835hg19UCSC Ensembl
Innerchr18:29948565..30081833hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38133269
hg19133269
hg18133269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878959
Samples
Known GenesNOL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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