A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595417



Internal ID20968488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124125579..124126484hg38UCSC Ensembl
chr11:123996286..123997191hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220329
Samples
Known GenesVWA5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595417
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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