A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391541



Internal ID22449411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15835364..15841487hg38UCSC Ensembl
chr2:15975488..15981611hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg386124
hg196124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885418
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391541
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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