A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555252



Internal ID20928343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174198040..174198547hg38UCSC Ensembl
chr2:175062768..175063275hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256134
Samples
Known GenesOLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555252
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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