A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542935



Internal ID21867290
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 StatusS
Merged Variantsnsv6106768
Supporting Variants
Samples
Known GenesATOH1, BMPR1B, GRID2, HPGDS, PDLIM5, SMARCAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542935
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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