A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546931



Internal ID20920142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85658327..85658928hg38UCSC Ensembl
chr1:86124010..86124611hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253938
Samples
Known GenesZNHIT6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546931
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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