A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988151



Internal ID20555191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129716696..129754903hg38UCSC Ensembl
chr11:129586591..129624798hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3838208
hg1938208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469403
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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