A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574833



Internal ID20947904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:58185011..58192517hg38UCSC Ensembl
chr4:59051177..59058683hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg387507
hg197507
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574833
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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