A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565950



Internal ID20939021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120814756..120819014hg38UCSC Ensembl
chr6:121135902..121140160hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384259
hg194259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6379n223
Supporting Variantsnssv18269238
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565950
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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