A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1568



Internal ID15199445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:63996338..64053094hg38UCSC Ensembl
Outerchr15:64288537..64345293hg19UCSC Ensembl
Outerchr15:62075590..62132346hg18UCSC Ensembl
Outerchr15:62075590..62132346hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg386176
hg196176
hg186176
hg176176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2939, nssv10057
SamplesNA18956, NA18555
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)nsv1568
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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