A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10964



Internal ID15539552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:85382581..85415085hg38UCSC Ensembl
Outerchr16:85416187..85448691hg19UCSC Ensembl
Outerchr16:83973688..84006192hg18UCSC Ensembl
Outerchr16:83973688..84006192hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3832505
hg1932505
hg1832505
hg1732505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1913
Supporting Variants
SamplesNA15510
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv10964
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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