A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543271



Internal ID20916523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85658465..85658712hg38UCSC Ensembl
chr1:86124148..86124395hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253939
Samples
Known GenesZNHIT6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543271
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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