A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432220



Internal ID22490090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101804291..101804368hg38UCSC Ensembl
chr8:102816519..102816596hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918177
Supporting Variants
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432220
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00


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