A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538756



Internal ID20912070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161991406..161991695hg38UCSC Ensembl
chr2:162847916..162848205hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538756
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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