A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993481



Internal ID19232112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:31745229..31750677hg38UCSC Ensembl
Outerchr21:33117542..33122990hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg385449
hg195449
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141970
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993481
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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