A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516237



Internal ID15096844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24324556..24330152hg38UCSC Ensembl
Innerchr14:24793762..24799358hg19UCSC Ensembl
Innerchr14:23863602..23869198hg18UCSC Ensembl
Innerchr14:23863602..23869198hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385597
hg195597
hg185597
hg175597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682128, nssv666991, nssv686806, nssv669111, nssv670608
Samples
Known GenesADCY4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516237
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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