A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536782



Internal ID20910125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55218852..55219709hg38UCSC Ensembl
chr1:55684525..55685382hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536782
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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