A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948980



Internal ID22724442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16476902..16476902hg38UCSC Ensembl
chr10:16518901..16518901hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368887
Samples
Known GenesPTER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948980
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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