A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586879



Internal ID20959950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30291088..30291680hg38UCSC Ensembl
chr10:30580017..30580609hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586879
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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