A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901382



Internal ID22676532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11914401..12871932hg38UCSC Ensembl
chr3:11955875..12913431hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg38957532
hg19957557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392296
Samples
Known GenesC3orf83, CAND2, MKRN2, PPARG, RAF1, RPL32, SNORA7A, SYN2, TIMP4, TMEM40, TSEN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901382
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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