A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903712



Internal ID22678881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182949313..182949670hg38UCSC Ensembl
chr3:182667101..182667458hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424224
Samples
Known GenesDCUN1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903712
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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