A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573788



Internal ID20946859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86432631..86433649hg38UCSC Ensembl
chr8:87444860..87445878hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278937
Samples
Known GenesWWP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573788
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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