A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2112



Internal ID15194709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68172970..68204223hg38UCSC Ensembl
Outerchr15:68465308..68496561hg19UCSC Ensembl
Outerchr15:66252362..66283615hg18UCSC Ensembl
Outerchr15:66252362..66283615hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388772
hg198772
hg188772
hg178772
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1581
Supporting Variants
SamplesNA18555
Known GenesCALML4, PIAS1
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)nssv2112
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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