A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987323



Internal ID20554365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12605121..12609808hg38UCSC Ensembl
chr11:12626668..12631355hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg384688
hg194688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451587
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987323
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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