A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515770



Internal ID15442827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1257675..1299928hg38UCSC Ensembl
Innerchr16:1307676..1349929hg19UCSC Ensembl
Innerchr16:1247677..1289930hg18UCSC Ensembl
Innerchr16:1247677..1289930hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3842254
hg1942254
hg1842254
hg1742254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666944, nssv689261, nssv664730, nssv673963, nssv679993, nssv680881
Samples
Known GenesTPSD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515770
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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