A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552793



Internal ID20925920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176435791..176441260hg38UCSC Ensembl
chr2:177300519..177305988hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg385470
hg195470
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256189
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552793
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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