A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444883



Internal ID22502753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:118806838..118809386hg38UCSC Ensembl
chr8:119819077..119821625hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg382549
hg192549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910137
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444883
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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