A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685711



Internal ID21207570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28430944..28431148hg38UCSC Ensembl
chr11:28452491..28452695hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790345
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685711
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.296875


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