A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903808



Internal ID22678979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51849893..51849958hg38UCSC Ensembl
chr3:51883909..51883974hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903808
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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