A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545715



Internal ID15986438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:18346280..18403811hg38UCSC Ensembl
Innerchr1:18672774..18730305hg19UCSC Ensembl
Innerchr1:18545361..18602892hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3857532
hg1957532
hg1857532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv711244
Samples
Known GenesIGSF21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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