A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7196



Internal ID15189982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:73903279..73936860hg38UCSC Ensembl
Outerchr15:74195620..74229201hg19UCSC Ensembl
Outerchr15:71982673..72016254hg18UCSC Ensembl
Outerchr15:71982673..72016254hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg385856
hg195856
hg185856
hg175856
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1604
Supporting Variants
SamplesNA12156
Known GenesLOXL1, LOXL1-AS1
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)nssv7196
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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