A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584628



Internal ID16372037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:228438026..228480036hg38UCSC Ensembl
Innerchr2:229302742..229344752hg19UCSC Ensembl
Innerchr2:229010986..229052996hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3842011
hg1942011
hg1842011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150746
SamplesHGDP01215
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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