A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1612



Internal ID15199489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74955384..74988943hg38UCSC Ensembl
Outerchr15:75247725..75281284hg19UCSC Ensembl
Outerchr15:73034778..73068337hg18UCSC Ensembl
Outerchr15:73034778..73068337hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3833560
hg1933560
hg1833560
hg1733560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7198
SamplesNA12156
Known GenesRPP25
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)nsv1612
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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