A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443503



Internal ID22501373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26611293..26611432hg38UCSC Ensembl
chr7:26650912..26651051hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926697
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443503
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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