A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540229



Internal ID20913521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85565348..85565883hg38UCSC Ensembl
chr2:85792471..85793006hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540229
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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