A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567006



Internal ID20940077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2619725..2620797hg38UCSC Ensembl
chr4:2621452..2622524hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381073
hg191073
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567006
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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