A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1324



Internal ID15544394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:76015717..76024065hg38UCSC Ensembl
Outerchr16:76049615..76057963hg19UCSC Ensembl
Outerchr16:74607116..74615464hg18UCSC Ensembl
Outerchr16:74607116..74615464hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg387440
hg197440
hg187440
hg177440
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1882
Supporting Variants
SamplesNA19240
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)nssv1324
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer