A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350117



Internal ID22575786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114246525..114246525hg38UCSC Ensembl
chr10:116006284..116006284hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963863
Supporting Variants
Samples
Known GenesVWA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350117
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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