A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994965



Internal ID64075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26290462..26320723hg38UCSC Ensembl
chr7:26330082..26360343hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3830262
hg1930262
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493252
Supporting Variants
Samples
Known GenesSNX10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994965
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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