A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570421



Internal ID20943492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84865035..84866009hg38UCSC Ensembl
chr4:85786188..85787162hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5349n223
Supporting Variantsnssv18266072
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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