A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392593



Internal ID22450463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218930421..218932337hg38UCSC Ensembl
chr2:219795143..219797059hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381917
hg191917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392593
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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