A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441696



Internal ID22499566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83170913..83171236hg38UCSC Ensembl
chr7:82800229..82800552hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909528
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441696
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005


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