A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2149



Internal ID15194746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75168488..75220390hg38UCSC Ensembl
Outerchr16:75202386..75254288hg19UCSC Ensembl
Outerchr16:73759887..73811789hg18UCSC Ensembl
Outerchr16:73759887..73811789hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3851903
hg1951903
hg1851903
hg1751903
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA18555
Known GenesCTRB1, CTRB2, ZFP1
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)nssv2149
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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