A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577483



Internal ID20950554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90721411..90721943hg38UCSC Ensembl
chr15:91264642..91265174hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2627n223
Supporting Variantsnssv18240587
Samples
Known GenesBLM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577483
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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