A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1682



Internal ID15546245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:96459855..96504981hg38UCSC Ensembl
Outerchr15:97003085..97048211hg19UCSC Ensembl
Outerchr15:94804089..94849215hg18UCSC Ensembl
Outerchr15:94804089..94849215hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3845127
hg1945127
hg1845127
hg1745127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7218
SamplesNA12156
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)nsv1682
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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