A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351507



Internal ID22577176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102493001..102493001hg38UCSC Ensembl
chr10:104252758..104252758hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963075
Supporting Variants
Samples
Known GenesACTR1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351507
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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