A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564121



Internal ID20937192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94710958..94711752hg38UCSC Ensembl
chr4:95632109..95632903hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564121
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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