A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364923



Internal ID22590592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2639383..2639455hg38UCSC Ensembl
chr1:2570822..2570894hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872917
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364923
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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