A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4162



Internal ID15538889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:71359192..71381435hg38UCSC Ensembl
Outerchr15:71651531..71673774hg19UCSC Ensembl
Outerchr15:69438585..69460828hg18UCSC Ensembl
Outerchr15:69438585..69460828hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384844
hg194844
hg184844
hg174844
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1598
Supporting Variants
SamplesNA12878
Known GenesTHSD4
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)nssv4162
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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