A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546315



Internal ID15987038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:58783359..58784264hg38UCSC Ensembl
Innerchr1:59249031..59249936hg19UCSC Ensembl
Innerchr1:59021619..59022524hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38906
hg19906
hg18906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv715266, nssv715267, nssv715268
Samples
Known GenesJUN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546315
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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