A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6561



Internal ID15190617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:52285869..52488521hg38UCSC Ensembl
Outerchr13:52860004..53062656hg19UCSC Ensembl
Outerchr13:51758005..51960657hg18UCSC Ensembl
Outerchr13:51758005..51960657hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38202653
hg19202653
hg18202653
hg17202653
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7242
Supporting Variants
SamplesNA12156
Known GenesCKAP2, THSD1, VPS36
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)nssv6561
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