A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7158



Internal ID15536706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:38426597..38471658hg38UCSC Ensembl
Outerchr15:38718798..38763859hg19UCSC Ensembl
Outerchr15:36506090..36551151hg18UCSC Ensembl
Outerchr15:36506090..36551151hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3845062
hg1945062
hg1845062
hg1745062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1500
Supporting Variants
SamplesNA12156
Known GenesFAM98B
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)nssv7158
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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