A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537594



Internal ID312845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9926174..9926216hg38UCSC Ensembl
chr3:9967858..9967900hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929408
Samples
Known GenesIL17RC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537594
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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