A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555189



Internal ID20928279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207679961..207681224hg38UCSC Ensembl
chr2:208544685..208545948hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555189
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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