A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560585



Internal ID20933656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52741693..52747212hg38UCSC Ensembl
chr6:52606491..52612010hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg385520
hg195520
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271500
Samples
Known GenesGSTA7P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560585
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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