A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408671



Internal ID22466541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34758467..34758568hg38UCSC Ensembl
chr22:35154458..35154559hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408671
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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