A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918883



Internal ID22694105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26548604..26548714hg38UCSC Ensembl
chr7:26588223..26588333hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918883
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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