A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983594



Internal ID18890502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:114227247..114230867hg38UCSC Ensembl
Outerchr6:114548411..114552031hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383621
hg193621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125421
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983594
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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