A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557989



Internal ID20931060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121571074..121575810hg38UCSC Ensembl
chr6:121892220..121896956hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384737
hg194737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557989
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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