A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9534



Internal ID15193094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75206812..75259199hg38UCSC Ensembl
Outerchr16:75240710..75293097hg19UCSC Ensembl
Outerchr16:73798211..73850598hg18UCSC Ensembl
Outerchr16:73798211..73850598hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3852388
hg1952388
hg1852388
hg1752388
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA18507
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)nssv9534
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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