A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584898



Internal ID16372307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240923534..240924859hg38UCSC Ensembl
Innerchr2:241862951..241864276hg19UCSC Ensembl
Innerchr2:241511624..241512949hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381326
hg191326
hg181326
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7380n54
Supporting Variantsnssv934143, nssv934151, nssv934145, nssv934157, nssv934163, nssv934142, nssv934171, nssv934125, nssv934134, nssv934152, nssv934141, nssv934124, nssv934172, nssv934132, nssv934168, nssv934170, nssv934139, nssv934159, nssv934162, nssv934140, nssv934128, nssv934130, nssv934144, nssv934154, nssv934160, nssv934133, nssv934167, nssv934164, nssv934129, nssv934150, nssv934138, nssv934166, nssv934136, nssv934153, nssv934149, nssv934158, nssv934127, nssv934126, nssv934169, nssv934135, nssv934131, nssv934148, nssv934155, nssv934161, nssv934147, nssv934146, nssv934173, nssv934156, nssv934165, nssv934137
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584898
Frequency
Sample Size17421
Observed Gain29
Observed Loss21
Observed Complex0
Frequencyn/a


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