A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516023



Internal ID15096630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24020396..24081015hg38UCSC Ensembl
Innerchr14:24489605..24550224hg19UCSC Ensembl
Innerchr14:23559445..23620064hg18UCSC Ensembl
Innerchr14:23559445..23620064hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3860620
hg1960620
hg1860620
hg1760620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682486, nssv685511, nssv691221, nssv665776, nssv696637, nssv678429
Samples
Known GenesCPNE6, DHRS4L1, LRRC16B, NRL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516023
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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