A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537978



Internal ID20911305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218765908..218766374hg38UCSC Ensembl
chr2:219630631..219631097hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537978
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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