A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106768



Internal ID22016001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92017603..94765936hg38UCSC Ensembl
chr4:92938754..95687087hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382748334
hg192748334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542935
Samples
Known GenesATOH1, BMPR1B, GRID2, HPGDS, PDLIM5, SMARCAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106768
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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