A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594526



Internal ID20967597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98090312..99013053hg38UCSC Ensembl
chr15:98633541..99556282hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38922742
hg19922742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2644n223
Supporting Variantsnssv18239140
Samples
Known GenesFAM169B, IGF1R, MIR4714, PGPEP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594526
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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