A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14454675



Internal ID22270008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63716793..63769525hg38UCSC Ensembl
chr13:64290926..64343658hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3852733
hg1952733
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3231163
Supporting Variants
SamplesNA19239
Known GenesLINC00395, OR7E156P
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14454675
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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