A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987864



Internal ID19215220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:20566628..20566714hg38UCSC Ensembl
Outerchr16:20577950..20578036hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133055
Supporting Variants
SamplesKWS1
Known GenesACSM2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987864
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