A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5631



Internal ID15197121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:3060187..3205399hg38UCSC Ensembl
Outerchr17:2963481..3108693hg19UCSC Ensembl
Outerchr17:2910231..3055443hg18UCSC Ensembl
Outerchr17:2910231..3055443hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38145213
hg19145213
hg18145213
hg17145213
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7288
Supporting Variants
SamplesNA19129
Known GenesOR1A2, OR1D2, OR1D5, OR1G1
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)nssv5631
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