A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485435



Internal ID262824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40229252..40280282hg38UCSC Ensembl
chr7:40268851..40319881hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3851031
hg1951031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994741
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485435
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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