A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548632



Internal ID20921816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39424113..39424547hg38UCSC Ensembl
chr2:39651254..39651688hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260235
Samples
Known GenesMAP4K3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548632
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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