A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004370



Internal ID70553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138329441..138368053hg38UCSC Ensembl
chr7:138014186..138052798hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3838613
hg1938613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491278
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004370
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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