A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548379



Internal ID20921566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90983872..90984457hg38UCSC Ensembl
chr1:91449429..91450014hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252005
Samples
Known GenesZNF644
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548379
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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