A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415202



Internal ID22473072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151081316..151081466hg38UCSC Ensembl
chr3:150799103..150799253hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895013
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415202
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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