A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580618



Internal ID20953689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68057612..68057737hg38UCSC Ensembl
chr10:69817369..69817494hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220170
Samples
Known GenesHERC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580618
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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