A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435448



Internal ID22493318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132868912..132869187hg38UCSC Ensembl
chr8:133881157..133881432hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924959
Supporting Variants
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435448
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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