A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395439



Internal ID22453309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38447972..38451414hg38UCSC Ensembl
chr2:38675114..38678556hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg383443
hg193443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869996
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395439
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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