A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261051



Internal ID20828091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157595985..157596923hg38UCSC Ensembl
chr3:157313774..157314712hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568046
Supporting Variants
Samples
Known GenesC3orf55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261051
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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