A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562421



Internal ID20935492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87591711..87592668hg38UCSC Ensembl
chr6:88301429..88302386hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274867
Samples
Known GenesORC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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