A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579706



Internal ID20952777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90721553..90721748hg38UCSC Ensembl
chr15:91264784..91264979hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240588
Samples
Known GenesBLM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579706
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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