A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10048



Internal ID15196063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43567062..43680265hg38UCSC Ensembl
Outerchr15:43859260..43972463hg19UCSC Ensembl
Outerchr15:41646552..41759755hg18UCSC Ensembl
Outerchr15:41646552..41759755hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38113204
hg19113204
hg18113204
hg17113204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1514
Supporting Variants
SamplesNA18956
Known GenesCATSPER2, CKMT1B, PPIP5K1, RNU6-28P, STRC
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)nssv10048
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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