A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586992



Internal ID20960063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63062298..63062935hg38UCSC Ensembl
chr10:64822058..64822695hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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