A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125307



Internal ID19286692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:20468936..20556259hg38UCSC Ensembl
Outerchr16:20480258..20567581hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3887324
hg1987324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983479
SamplesKWS2
Known GenesACSM2A, ACSM2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125307
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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