A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9520



Internal ID15193108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:1205108..1245512hg38UCSC Ensembl
Outerchr16:1255108..1295513hg19UCSC Ensembl
Outerchr16:1195109..1235514hg18UCSC Ensembl
Outerchr16:1195109..1235514hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3840405
hg1940406
hg1840406
hg1740406
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7274
Supporting Variants
SamplesNA18507
Known GenesCACNA1H, TPSAB1, TPSB2, TPSG1
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)nssv9520
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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