A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585025



Internal ID20958096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21671584..21672344hg38UCSC Ensembl
chr10:21960513..21961273hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235442
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585025
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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