A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426969



Internal ID205883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9999275..10000079hg38UCSC Ensembl
chr1:10059333..10060137hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891306
Samples
Known GenesRBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426969
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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