A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584100



Internal ID20957171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28040821..28091875hg38UCSC Ensembl
chr15:28285967..28337021hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3851055
hg1951055
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239425
Samples
Known GenesOCA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584100
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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