A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402434



Internal ID22460304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17844550..17844833hg38UCSC Ensembl
chr2:18025817..18026100hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877557
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402434
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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