A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493005



Internal ID270198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65997187..66017197hg38UCSC Ensembl
chr7:65462174..65482184hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3820011
hg1920011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493005
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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