A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983535



Internal ID18889257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:72342940..72347196hg38UCSC Ensembl
Outerchr15:72635281..72639537hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384257
hg194257
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125360
Supporting Variants
SamplesKWS2
Known GenesHEXA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983535
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