A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516851



Internal ID15444144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73246214..73271334hg38UCSC Ensembl
Innerchr14:73712922..73738042hg19UCSC Ensembl
Innerchr14:72782675..72807795hg18UCSC Ensembl
Innerchr14:72782675..72807795hg17UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3825121
hg1925121
hg1825121
hg1725121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661271, nssv690264, nssv660177, nssv663723, nssv654441, nssv692934, nssv676847, nssv682593
Samples
Known GenesPAPLN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516851
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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