A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266069



Internal ID20833109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84674672..84675170hg38UCSC Ensembl
chr4:85595825..85596323hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573661
Supporting Variants
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266069
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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