A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570778



Internal ID20943849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:124876381..124877571hg38UCSC Ensembl
chr4:125797536..125798726hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5438n223
Supporting Variantsnssv18263691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570778
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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