A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395839



Internal ID22453709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29069042..29069102hg38UCSC Ensembl
chr21:30441363..30441423hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950904
Supporting Variants
Samples
Known GenesCCT8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395839
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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