A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960884



Internal ID19217105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10076452..10076518hg38UCSC Ensembl
Outerchr21:10554480..10554546hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120129
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960884
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