A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572187



Internal ID20945258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149561534..149561787hg38UCSC Ensembl
chr6:149882670..149882923hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269271
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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