A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1578



Internal ID15199455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:67827799..67862385hg38UCSC Ensembl
Outerchr15:68120137..68154723hg19UCSC Ensembl
Outerchr15:65907191..65941777hg18UCSC Ensembl
Outerchr15:65907191..65941777hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385157
hg195157
hg185157
hg175157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4158
SamplesNA12878
Known GenesSKOR1
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)nsv1578
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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