A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987180



Internal ID20554222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118139470..118144865hg38UCSC Ensembl
chr11:118010185..118015580hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385396
hg195396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468101
Supporting Variants
Samples
Known GenesSCN4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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