A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913442



Internal ID22688658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46645418..46645867hg38UCSC Ensembl
chr11:46666968..46667417hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367997
Samples
Known GenesATG13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913442
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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