A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4167



Internal ID15192208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:78617170..78649604hg38UCSC Ensembl
Outerchr15:78909512..78941946hg19UCSC Ensembl
Outerchr15:76696567..76729001hg18UCSC Ensembl
Outerchr15:76696567..76729001hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg387294
hg197294
hg187294
hg177294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1628
Supporting Variants
SamplesNA12878
Known GenesCHRNA3, CHRNB4
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)nssv4167
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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