A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429936



Internal ID22487806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27715589..27715818hg38UCSC Ensembl
chr8:27573106..27573335hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918835
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429936
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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