A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538234



Internal ID20911555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26249476..26249996hg38UCSC Ensembl
chr2:26472344..26472864hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257533
Samples
Known GenesHADHB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538234
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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