A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5567



Internal ID15543884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76039762..76060777hg38UCSC Ensembl
Outerchr15:76332103..76353118hg19UCSC Ensembl
Outerchr15:74119158..74140173hg18UCSC Ensembl
Outerchr15:74119158..74140173hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3821016
hg1921016
hg1821016
hg1721016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1617
Supporting Variants
SamplesNA19129
Known GenesC15orf27
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)nssv5567
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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