A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478725



Internal ID256272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74770689..74954889hg38UCSC Ensembl
chr7:74185036..74369774hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38184201
hg19184739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17001005
Samples
Known GenesGTF2IRD2, NCF1, PMS2P5, STAG3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478725
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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