A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177449



Internal ID20744489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33330110..33543863hg38UCSC Ensembl
chr11:33351656..33565409hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38213754
hg19213754
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468680
Supporting Variants
Samples
Known GenesHIPK3, KIAA1549L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177449
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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