A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987861



Internal ID20554901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125117106..125124611hg38UCSC Ensembl
chr11:124987002..124994507hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg387506
hg197506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458481
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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