A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001015



Internal ID68248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74817389..74838779hg38UCSC Ensembl
chr7:74231918..74253899hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3821391
hg1921982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477223
Supporting Variants
Samples
Known GenesGTF2IRD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001015
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001257


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