A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542697



Internal ID20915955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179270679..179271561hg38UCSC Ensembl
chr1:179239814..179240696hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542697
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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