A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488837



Internal ID266130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74974779..74984779hg38UCSC Ensembl
chr7:74388929..74398921hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3810001
hg199993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488837
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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