A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979050



Internal ID19240212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:27579264..27595051hg38UCSC Ensembl
Outerchr3:27620755..27636542hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3815788
hg1915788
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140341
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979050
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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