A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17393205



Internal ID22451075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224672337..224681202hg38UCSC Ensembl
chr2:225537054..225545919hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg388866
hg198866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17393205
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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