A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9422



Internal ID15193687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:179643249..179682452hg38UCSC Ensembl
Outerchr5:179070250..179109453hg19UCSC Ensembl
Outerchr5:179002856..179042059hg18UCSC Ensembl
Outerchr5:179002856..179042059hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3839204
hg1939204
hg1839204
hg1739204
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7375
Supporting Variants
SamplesNA18517
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)nssv9422
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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