A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573807



Internal ID20946878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176800227..176800804hg38UCSC Ensembl
chr4:177721381..177721958hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573807
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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