A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9250



Internal ID15534614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20616533..20661199hg38UCSC Ensembl
Outerchr15:20821835..20866528hg19UCSC Ensembl
Outerchr15:19081849..19126542hg18UCSC Ensembl
Outerchr15:19081849..19126542hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3844667
hg1944694
hg1844694
hg1744694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1452
Supporting Variants
SamplesNA12156
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)nssv9250
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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