A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1619



Internal ID15199496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76312275..76346029hg38UCSC Ensembl
Outerchr15:76604616..76638370hg19UCSC Ensembl
Outerchr15:74391671..74425425hg18UCSC Ensembl
Outerchr15:74391671..74425425hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg385686
hg195686
hg185686
hg175686
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7200
SamplesNA12156
Known GenesISL2
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)nsv1619
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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