A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568430



Internal ID20941501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119357602..119358353hg38UCSC Ensembl
chr6:119678767..119679518hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568430
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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