A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538236



Internal ID20911557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191229680..191230028hg38UCSC Ensembl
chr2:192094406..192094754hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538236
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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