A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485680



Internal ID263064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107864186..107864490hg38UCSC Ensembl
chr7:107504631..107504935hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485680
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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