A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591848



Internal ID20964919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21659575..21660616hg38UCSC Ensembl
chr10:21948504..21949545hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217862
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591848
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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