A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444183



Internal ID22502053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38077591..38080749hg38UCSC Ensembl
chr8:37935109..37938267hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383159
hg193159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444183
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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