A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118564



Internal ID21404271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36257656..36257725hg38UCSC Ensembl
chr21:37629954..37630023hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588248
Supporting Variants
SamplesHG00512
Known GenesDOPEY2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118564
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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