A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978695



Internal ID19229165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:40388246..40403785hg38UCSC Ensembl
Outerchr14:40857450..40872989hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3815540
hg1915540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116510
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978695
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