A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421681



Internal ID22479551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149210172..149227712hg38UCSC Ensembl
chr3:148927959..148945499hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3817541
hg1917541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896507
Supporting Variants
Samples
Known GenesCP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421681
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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