A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11097



Internal ID15539611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:658779..787671hg38UCSC Ensembl
Outerchr5:658894..787786hg19UCSC Ensembl
Outerchr5:711894..840786hg18UCSC Ensembl
Outerchr5:711894..840786hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38128893
hg19128893
hg18128893
hg17128893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4675
Supporting Variants
SamplesNA15510
Known GenesTPPP
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)nssv11097
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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