A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355063



Internal ID22580732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118423950..118423950hg38UCSC Ensembl
chr10:120183462..120183462hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355063
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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