A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545351



Internal ID20918582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90788655..90789231hg38UCSC Ensembl
chr1:91254212..91254788hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251995
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545351
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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