A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578387



Internal ID20951458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70392469..70393024hg38UCSC Ensembl
chr10:72152225..72152780hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578387
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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