A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552153



Internal ID20925283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:182613414..182614557hg38UCSC Ensembl
chr2:183478141..183479284hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg381144
hg191144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552153
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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