A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553922



Internal ID20927032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26803065..26803645hg38UCSC Ensembl
chr2:27025933..27026513hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553922
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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