A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994238



Internal ID63616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25435128..25435180hg38UCSC Ensembl
chr7:25474747..25474799hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141909
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994238
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008168


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