A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487969



Internal ID265291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66078957..66102342hg38UCSC Ensembl
chr7:65543944..65567329hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3823386
hg1923386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997617
Samples
Known GenesASL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487969
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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