A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1567



Internal ID15199444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:63898305..63922771hg38UCSC Ensembl
Outerchr15:64190504..64214970hg19UCSC Ensembl
Outerchr15:61977557..62002023hg18UCSC Ensembl
Outerchr15:61977557..62002023hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3824467
hg1924467
hg1824467
hg1724467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7185
SamplesNA12156
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)nsv1567
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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