A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574456



Internal ID20947527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94120961..94121106hg38UCSC Ensembl
chr4:95042112..95042257hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265411
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574456
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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