A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183157



Internal ID20750197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62744969..62751397hg38UCSC Ensembl
chr11:62512441..62518869hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg386429
hg196429
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455813
Supporting Variants
Samples
Known GenesZBTB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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