A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990235



Internal ID20557276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29525699..29527201hg38UCSC Ensembl
chr11:29547246..29548748hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381503
hg191503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438958
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990235
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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