A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753772



Internal ID21385935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:227458558..227459879hg38UCSC Ensembl
chr2:228323274..228324595hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg381322
hg191322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433701
Supporting Variants
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753772
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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