A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594747



Internal ID20967818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62469181..62470401hg38UCSC Ensembl
chr11:62236653..62237873hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229925
Samples
Known GenesAHNAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594747
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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