A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595072



Internal ID20968143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19522440..19523833hg38UCSC Ensembl
chr11:19543987..19545380hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381394
hg191394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219546
Samples
Known GenesNAV2, NAV2-AS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595072
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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