A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2150



Internal ID15194747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75205730..75263709hg38UCSC Ensembl
Outerchr16:75239628..75297607hg19UCSC Ensembl
Outerchr16:73797129..73855108hg18UCSC Ensembl
Outerchr16:73797129..73855108hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3857980
hg1957980
hg1857980
hg1757980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA18555
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)nssv2150
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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