A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546362



Internal ID15987085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59585122..59586603hg38UCSC Ensembl
Innerchr1:60050794..60052275hg19UCSC Ensembl
Innerchr1:59823382..59824863hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg381482
hg191482
hg181482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv715479
Samples
Known GenesFGGY
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546362
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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