A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575977



Internal ID20949048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63244898..63245701hg38UCSC Ensembl
chr10:65004658..65005461hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222777
Samples
Known GenesJMJD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575977
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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