A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790399



Internal ID21235737
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 StatusM
Merged Variants
Supporting Variantsnssv13689865
Samples
Known GenesRRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790399
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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