A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584804



Internal ID16372213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240186202..240237001hg38UCSC Ensembl
Innerchr2:241125619..241176418hg19UCSC Ensembl
Innerchr2:240774292..240825091hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3850800
hg1950800
hg1850800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151186
SamplesHGDP00971
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584804
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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