A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589635



Internal ID20962706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76272270..76273403hg38UCSC Ensembl
chr15:76564611..76565744hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg381134
hg191134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2588n223
Supporting Variantsnssv18242014
Samples
Known GenesETFA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589635
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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