A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597449



Internal ID20970520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8060321..8060786hg38UCSC Ensembl
chr19:8125205..8125670hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246490
Samples
Known GenesCCL25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597449
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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