A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9959



Internal ID15540051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76040482..76067094hg38UCSC Ensembl
Outerchr15:76332823..76359435hg19UCSC Ensembl
Outerchr15:74119878..74146490hg18UCSC Ensembl
Outerchr15:74119878..74146490hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3826613
hg1926613
hg1826613
hg1726613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1617
Supporting Variants
SamplesNA18507
Known GenesC15orf27
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)nssv9959
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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