A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540413



Internal ID20913704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156408140..156408716hg38UCSC Ensembl
chr2:157264652..157265228hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4158n223
Supporting Variantsnssv18255291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540413
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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