A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4227



Internal ID15192268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75216003..75251207hg38UCSC Ensembl
Outerchr16:75249901..75285105hg19UCSC Ensembl
Outerchr16:73807402..73842606hg18UCSC Ensembl
Outerchr16:73807402..73842606hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3835205
hg1935205
hg1835205
hg1735205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA12878
Known GenesBCAR1, CTRB1
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)nssv4227
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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