A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10057



Internal ID15196054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:63996338..64027819hg38UCSC Ensembl
Outerchr15:64288537..64320018hg19UCSC Ensembl
Outerchr15:62075590..62107071hg18UCSC Ensembl
Outerchr15:62075590..62107071hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg388023
hg198023
hg188023
hg178023
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1568
Supporting Variants
SamplesNA18956
Known GenesDAPK2
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)nssv10057
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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