A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689865



Internal ID21211720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4137882..4138055hg38UCSC Ensembl
chr11:4159112..4159285hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790399
Supporting Variants
Samples
Known GenesRRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689865
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.796875


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