A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2118



Internal ID15194715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:77033054..77041255hg38UCSC Ensembl
Outerchr15:77325395..77333596hg19UCSC Ensembl
Outerchr15:75112450..75120651hg18UCSC Ensembl
Outerchr15:75112450..75120651hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg389820
hg199820
hg189820
hg179820
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1622
Supporting Variants
SamplesNA18555
Known GenesPSTPIP1
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)nssv2118
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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