A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535631



Internal ID20908989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171269034..171269534hg38UCSC Ensembl
chr2:172125544..172126044hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535631
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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