A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969899



Internal ID22744834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41981511..42344815hg38UCSC Ensembl
chr3:42023003..42386307hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38363305
hg19363305
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417511
Samples
Known GenesCCK, TRAK1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969899
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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