A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979019



Internal ID19226331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:311115..311705hg38UCSC Ensembl
Outerchr16:361115..361705hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125366
Supporting Variants
SamplesKWS2
Known GenesAXIN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979019
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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