A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9887



Internal ID15193278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:181126399..181160578hg38UCSC Ensembl
Outerchr5:180553399..180587578hg19UCSC Ensembl
Outerchr5:180486005..180520184hg18UCSC Ensembl
Outerchr5:180486005..180520184hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3834180
hg1934180
hg1834180
hg1734180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5163
Supporting Variants
SamplesNA18507
Known GenesOR2V2
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)nssv9887
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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