A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489463



Internal ID266742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90709528..90716388hg38UCSC Ensembl
chr7:90338842..90345702hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg386861
hg196861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999593
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489463
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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