A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10961



Internal ID15192863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75207094..75264317hg38UCSC Ensembl
Outerchr16:75240992..75298215hg19UCSC Ensembl
Outerchr16:73798493..73855716hg18UCSC Ensembl
Outerchr16:73798493..73855716hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3857224
hg1957224
hg1857224
hg1757224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA15510
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)nssv10961
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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