A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518245



Internal ID15445538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7806210..7813357hg38UCSC Ensembl
Innerchr16:7856212..7863359hg19UCSC Ensembl
Innerchr16:7796213..7803360hg18UCSC Ensembl
Innerchr16:7796213..7803360hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg387148
hg197148
hg187148
hg177148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695675
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518245
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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