A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592507



Internal ID20965578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50218206..50218403hg38UCSC Ensembl
chr15:50510403..50510600hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238080
Samples
Known GenesSLC27A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592507
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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