A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5615



Internal ID15197141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75206787..75261870hg38UCSC Ensembl
Outerchr16:75240685..75295768hg19UCSC Ensembl
Outerchr16:73798186..73853269hg18UCSC Ensembl
Outerchr16:73798186..73853269hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3855084
hg1955084
hg1855084
hg1755084
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA19129
Known GenesBCAR1, CTRB1, CTRB2
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)nssv5615
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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