A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582597



Internal ID20955668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51882017..51882517hg38UCSC Ensembl
chr15:52174214..52174714hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240350
Samples
Known GenesTMOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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