A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437281



Internal ID22495151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37788536..37788611hg38UCSC Ensembl
chr8:37646054..37646129hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437281
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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