A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv97



Internal ID15383571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20404857..22287907hg38UCSC Ensembl
Outerchr15:20610110..22575858hg19UCSC Ensembl
Outerchr15:18870124..20077222hg18UCSC Ensembl
Outerchr15:18870124..20077222hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381883051
hg191965749
hg181207099
hg171207099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv97
Supporting Variants
SamplesNA15510
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSequencing
AnalysisFosmids were categorized as discordant if the in silico size was in excess of three standard deviations from the mean (<32 or 48> kb) and/or showed incorrect orientation of ends
PlatformCapillary
Comments
ReferenceTuzun_et_al_2005
Pubmed ID15895083
Accession Number(s)nssv97
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer