A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225101



Internal ID20792141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33316529..33317281hg38UCSC Ensembl
chr11:33338075..33338827hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586725
Supporting Variants
Samples
Known GenesHIPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225101
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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