A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7192



Internal ID15536672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:69564946..69581565hg38UCSC Ensembl
Outerchr15:69857285..69873904hg19UCSC Ensembl
Outerchr15:67644339..67660958hg18UCSC Ensembl
Outerchr15:67644339..67660958hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385570
hg195570
hg185570
hg175570
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1587
Supporting Variants
SamplesNA12156
Known GenesLOC145837
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)nssv7192
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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