A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588916



Internal ID20961987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68792975..68794195hg38UCSC Ensembl
chr10:70552732..70553952hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588916
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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