A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978711



Internal ID19243330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:21152202..21158308hg38UCSC Ensembl
Outerchr2:21375074..21381180hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg386107
hg196107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116530
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978711
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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