A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407056



Internal ID22464926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15016319..15057662hg38UCSC Ensembl
chr2:15156443..15197786hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3841344
hg1941344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871815
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407056
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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