A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487172



Internal ID264516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61519000..61654000hg38UCSC Ensembl
chr9:44726838..44861838hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38135001
hg19135001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487172
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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