A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544938



Internal ID20918176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149197347..149198047hg38UCSC Ensembl
chr2:150053861..150054561hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254558
Samples
Known GenesLYPD6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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