A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570333



Internal ID20943404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15040554..15042519hg38UCSC Ensembl
chr6:15040785..15042750hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381966
hg191966
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570333
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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