A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545595



Internal ID16333004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15683361..15683999hg38UCSC Ensembl
Innerchr1:16009856..16010494hg19UCSC Ensembl
Innerchr1:15882443..15883081hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38639
hg19639
hg18639
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv710499, nssv710498
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545595
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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