A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538064



Internal ID20911390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191558937..191559398hg38UCSC Ensembl
chr2:192423663..192424124hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538064
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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