A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569592



Internal ID20942663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4092807..4094430hg38UCSC Ensembl
chr6:4093041..4094664hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381624
hg191624
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271433
Samples
Known GenesC6orf201
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569592
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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