A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922057



Internal ID22697282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11976169..11993056hg38UCSC Ensembl
chr7:12015795..12032682hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3816888
hg1916888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922057
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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