A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364604



Internal ID22590273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10805656..10805746hg38UCSC Ensembl
chr11:10827203..10827293hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924707
Supporting Variants
Samples
Known GenesEIF4G2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364604
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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