A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537707



Internal ID20911042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69702030..69702598hg38UCSC Ensembl
chr2:69929162..69929730hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258905
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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