A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429953



Internal ID22487823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20556174..20556380hg38UCSC Ensembl
chr8:20413685..20413891hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429953
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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