A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746677



Internal ID21385009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36303613..36304002hg38UCSC Ensembl
chr21:37675911..37676300hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433350
Supporting Variants
SamplesBTQ038
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746677
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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