A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570574



Internal ID20943645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63871532..63872647hg38UCSC Ensembl
chr6:64581425..64582540hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381116
hg191116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273923
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570574
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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