A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898385



Internal ID22673499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141786548..141790414hg38UCSC Ensembl
chr3:141505390..141509256hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383867
hg193867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393440
Samples
Known GenesGRK7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898385
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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