A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588754



Internal ID20961825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43440421..43442191hg38UCSC Ensembl
chr15:43732619..43734389hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg381771
hg191771
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2510n223
Supporting Variantsnssv18239560
Samples
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588754
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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