A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361546



Internal ID22587215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62751274..62751807hg38UCSC Ensembl
chr11:62518746..62519279hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924725
Supporting Variants
Samples
Known GenesZBTB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361546
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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