A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6660



Internal ID15190518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14878956..15027600hg38UCSC Ensembl
Outerchr16:14972813..15121457hg19UCSC Ensembl
Outerchr16:14880314..15028958hg18UCSC Ensembl
Outerchr16:14880314..15028958hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38148645
hg19148645
hg18148645
hg17148645
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7277
Supporting Variants
SamplesNA12156
Known GenesLOC100288162, MIR1972-1, MIR1972-2, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, PDXDC1
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)nssv6660
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