A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979031



Internal ID18879500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:47338515..47338592hg38UCSC Ensembl
Outerchr19:47841772..47841849hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140320
Supporting Variants
SamplesKWS2
Known GenesC5AR2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979031
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