A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476325



Internal ID253939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107582438..107582499hg38UCSC Ensembl
chr7:107222883..107222944hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004037
Samples
Known GenesBCAP29
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476325
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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