A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581654



Internal ID16369063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43257417..43326810hg38UCSC Ensembl
Innerchr2:43484556..43553949hg19UCSC Ensembl
Innerchr2:43338060..43407453hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3869394
hg1969394
hg1869394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6829n54
Supporting Variantsnssv1150424
SamplesNINDS_102
Known GenesTHADA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581654
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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