A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1654



Internal ID15546217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:88924726..88969104hg38UCSC Ensembl
Outerchr15:89467957..89512335hg19UCSC Ensembl
Outerchr15:87268961..87313339hg18UCSC Ensembl
Outerchr15:87268961..87313339hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3844379
hg1944379
hg1844379
hg1744379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4637
SamplesNA19129
Known Genes
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)nsv1654
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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