A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920970



Internal ID22696193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73769526..73769663hg38UCSC Ensembl
chr11:73480571..73480708hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359633
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920970
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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