A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229925



Internal ID20796966
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 StatusS
Merged Variantsnsv6594747
Supporting Variants
Samples
Known GenesAHNAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229925
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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