A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247292



Internal ID20814332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109071954..109072796hg38UCSC Ensembl
chr1:109614576..109615418hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536242
Supporting Variants
Samples
Known GenesTAF13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247292
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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