A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538413



Internal ID20911730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53706741..53707362hg38UCSC Ensembl
chr2:53933878..53934499hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258167
Samples
Known GenesASB3, GPR75-ASB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538413
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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