A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565068



Internal ID16352477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73062077..73080138hg38UCSC Ensembl
Innerchr14:73528785..73546846hg19UCSC Ensembl
Innerchr14:72598538..72616599hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3818062
hg1918062
hg1818062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3754n54
Supporting Variantsnssv829162, nssv829156, nssv829159, nssv829152, nssv829155, nssv829154, nssv829158, nssv829151, nssv829164, nssv829153, nssv829146, nssv829157, nssv829163, nssv829161, nssv829145, nssv829150, nssv829147, nssv829160, nssv829148, nssv829149
Samples
Known GenesRBM25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565068
Frequency
Sample Size17421
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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