A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993382



Internal ID19238701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:170170463..170171751hg38UCSC Ensembl
Outerchr5:169597467..169598755hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381289
hg191289
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125294
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993382
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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