A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961368



Internal ID19203943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:103734539..103748287hg38UCSC Ensembl
Outerchr3:103453383..103467131hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3813749
hg1913749
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110946
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961368
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