A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557284



Internal ID20930355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69220537..69274673hg38UCSC Ensembl
chr4:70086255..70140391hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3854137
hg1954137
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5319n223
Supporting Variantsnssv18265921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557284
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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