A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554991



Internal ID20928080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77320750..77323001hg38UCSC Ensembl
chr1:77786435..77788686hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382252
hg192252
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253151
Samples
Known GenesAK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554991
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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