A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545038



Internal ID15985761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1727506..1749003hg38UCSC Ensembl
Innerchr1:1658945..1680442hg19UCSC Ensembl
Innerchr1:1648805..1670302hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3821498
hg1921498
hg1821498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv42n54
Supporting Variantsnssv708633
Samples
Known GenesSLC35E2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545038
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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