A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3422



Internal ID15191464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26685198..26857543hg38UCSC Ensembl
Outerchr6:26685426..26825322hg19UCSC Ensembl
Outerchr6:26793405..26933301hg18UCSC Ensembl
Outerchr6:26793405..26933301hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38172346
hg19139897
hg18139897
hg17139897
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7378
Supporting Variants
SamplesNA12878
Known Genes
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)nssv3422
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