A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427668



Internal ID22485538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55733565..55733565hg38UCSC Ensembl
chr3:55767593..55767593hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958074
Supporting Variants
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427668
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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