A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420260



Internal ID22478130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150594592..150594892hg38UCSC Ensembl
chr3:150312379..150312679hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420260
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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