A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588344



Internal ID20961415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28414166..28414521hg38UCSC Ensembl
chr10:28703095..28703450hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588344
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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