A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1512



Internal ID15199389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43324636..43369448hg38UCSC Ensembl
Outerchr15:43616834..43661646hg19UCSC Ensembl
Outerchr15:41404126..41448938hg18UCSC Ensembl
Outerchr15:41404126..41448938hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3844813
hg1944813
hg1844813
hg1744813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7161
SamplesNA12156
Known GenesADAL, LCMT2, ZSCAN29
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)nsv1512
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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