A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564289



Internal ID20937360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127757324..127757744hg38UCSC Ensembl
chr8:128769570..128769990hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276223
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564289
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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