A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751144



Internal ID21387694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36303685..36303985hg38UCSC Ensembl
chr21:37675983..37676283hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433351
Supporting Variants
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751144
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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