A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545598



Internal ID15986321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15683361..15684330hg38UCSC Ensembl
Innerchr1:16009856..16010825hg19UCSC Ensembl
Innerchr1:15882443..15883412hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38970
hg19970
hg18970
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv147n54
Supporting Variantsnssv710502, nssv710505, nssv710504, nssv710503
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545598
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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