A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9307



Internal ID15193572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43586547..43680335hg38UCSC Ensembl
Outerchr15:43878745..43972533hg19UCSC Ensembl
Outerchr15:41666037..41759825hg18UCSC Ensembl
Outerchr15:41666037..41759825hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3893789
hg1993789
hg1893789
hg1793789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1514
Supporting Variants
SamplesNA18517
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)nssv9307
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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