A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580315



Internal ID20953386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123117218..123118357hg38UCSC Ensembl
chr10:124876734..124877873hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580315
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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