A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584606



Internal ID20957677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49437319..49438400hg38UCSC Ensembl
chr10:50645365..50646446hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584606
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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