A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6784



Internal ID15190394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:38742662..38780766hg38UCSC Ensembl
Outerchr19:39233302..39271406hg19UCSC Ensembl
Outerchr19:43925142..43963246hg18UCSC Ensembl
Outerchr19:43925142..43963246hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3838105
hg1938105
hg1838105
hg1738105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7307
Supporting Variants
SamplesNA12156
Known GenesCAPN12, LGALS7
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)nssv6784
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