A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6680



Internal ID15190498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75215051..75250608hg38UCSC Ensembl
Outerchr16:75248949..75284506hg19UCSC Ensembl
Outerchr16:73806450..73842007hg18UCSC Ensembl
Outerchr16:73806450..73842007hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3835558
hg1935558
hg1835558
hg1735558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA12156
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)nssv6680
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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