A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925368



Internal ID22700595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66158183..66166992hg38UCSC Ensembl
chr7:65623170..65631979hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg388810
hg198810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925368
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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