A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6655



Internal ID15190523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:1233743..1291100hg38UCSC Ensembl
Outerchr16:1283744..1341101hg19UCSC Ensembl
Outerchr16:1223745..1281102hg18UCSC Ensembl
Outerchr16:1223745..1281102hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3857358
hg1957358
hg1857358
hg1757358
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7274
Supporting Variants
SamplesNA12156
Known GenesTPSAB1, TPSD1
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)nssv6655
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer