A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559978



Internal ID20933049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52211627..52213156hg38UCSC Ensembl
chr4:53077793..53079322hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381530
hg191530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5264n223
Supporting Variantsnssv18266387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559978
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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