A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593801



Internal ID20966872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21466408..21466992hg38UCSC Ensembl
chr10:21755337..21755921hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593801
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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