A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555431



Internal ID20928518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39504071..39506802hg38UCSC Ensembl
chr2:39731212..39733943hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg382732
hg192732
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257896
Samples
Known GenesLOC728730
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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