A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896788



Internal ID22671884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141931213..141931292hg38UCSC Ensembl
chr3:141650055..141650134hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896788
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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