A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546376



Internal ID20919594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174216134..174216716hg38UCSC Ensembl
chr2:175080862..175081444hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256136
Samples
Known GenesOLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546376
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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