A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748756



Internal ID21387440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238591693..238593021hg38UCSC Ensembl
chr2:239500334..239501662hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381329
hg191329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433709
Supporting Variants
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748756
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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