A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430738



Internal ID22488608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81412314..81412752hg38UCSC Ensembl
chr7:81041630..81042068hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913923
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430738
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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