A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546890



Internal ID15987613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:100736666..100751050hg38UCSC Ensembl
Innerchr1:101202222..101216606hg19UCSC Ensembl
Innerchr1:100974810..100989194hg18UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3814385
hg1914385
hg1814385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv719666
Samples
Known GenesVCAM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546890
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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