A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548097



Internal ID15988820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165828729..165855929hg38UCSC Ensembl
Innerchr1:165797966..165825166hg19UCSC Ensembl
Innerchr1:164064590..164091790hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3827201
hg1927201
hg1827201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv727724
Samples
Known GenesUCK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548097
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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