A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391898



Internal ID22449768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38783437..38783576hg38UCSC Ensembl
chr2:39010579..39010718hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391898
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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