A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001056



Internal ID68284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75100779..75110834hg38UCSC Ensembl
chr7:74516570..74526624hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3810056
hg1910055
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142677
Supporting Variants
Samples
Known GenesGTF2IRD2, GTF2IRD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001056
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.374498


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