A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449353



Internal ID22507223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20108498..20116845hg38UCSC Ensembl
chr7:20148121..20156468hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg388348
hg198348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449353
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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