A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589932



Internal ID20963003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26131375..26143558hg38UCSC Ensembl
chr15:26376522..26388705hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3812184
hg1912184
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239404
Samples
Known GenesLINC00929
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589932
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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