A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1344



Internal ID15197686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:9072978..9105474hg38UCSC Ensembl
Outerchr17:8976295..9008791hg19UCSC Ensembl
Outerchr17:8917020..8949516hg18UCSC Ensembl
Outerchr17:8917020..8949516hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3832497
hg1932497
hg1832497
hg1732497
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7289
Supporting Variants
SamplesNA19240
Known GenesNTN1
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)nssv1344
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