A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570532



Internal ID20943603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87084082..87084686hg38UCSC Ensembl
chr6:87793800..87794404hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570532
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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