A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540781



Internal ID20914070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:154031993..154133475hg38UCSC Ensembl
chr2:154888506..154989988hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38101483
hg19101483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254642
Samples
Known GenesGALNT13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540781
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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