A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8199



Internal ID15535665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:174691923..174707120hg38UCSC Ensembl
Outerchr5:174118926..174134123hg19UCSC Ensembl
Outerchr5:174051532..174066729hg18UCSC Ensembl
Outerchr5:174051532..174066729hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3815198
hg1915198
hg1815198
hg1715198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5138
Supporting Variants
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)nssv8199
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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