A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559310



Internal ID20932381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4034991..4035701hg38UCSC Ensembl
chr6:4035225..4035935hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271428
Samples
Known GenesPRPF4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559310
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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