A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545781



Internal ID16333190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24190390..24196802hg38UCSC Ensembl
Innerchr1:24516880..24523292hg19UCSC Ensembl
Innerchr1:24389467..24395879hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386413
hg196413
hg186413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv711340
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545781
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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