A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4883



Internal ID15196301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:179641546..179689929hg38UCSC Ensembl
Outerchr5:179068547..179116930hg19UCSC Ensembl
Outerchr5:179001153..179049536hg18UCSC Ensembl
Outerchr5:179001153..179049536hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3848384
hg1948384
hg1848384
hg1748384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7375
Supporting Variants
SamplesNA19129
Known GenesC5orf60, CBY3
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)nssv4883
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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