A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490547



Internal ID267800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106628420..106629188hg38UCSC Ensembl
chr7:106268866..106269634hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490547
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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