A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575158



Internal ID20948229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120360932..120361441hg38UCSC Ensembl
chr6:120682078..120682587hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575158
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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