A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1913



Internal ID15546476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:85382581..85421196hg38UCSC Ensembl
Outerchr16:85416187..85454802hg19UCSC Ensembl
Outerchr16:83973688..84012303hg18UCSC Ensembl
Outerchr16:83973688..84012303hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3838616
hg1938616
hg1838616
hg1738616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10964, nssv5619, nssv6688, nssv1331, nssv2154
SamplesNA12156, NA15510, NA18555, NA19240, NA19129
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)nsv1913
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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