A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967010



Internal ID22741945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30617674..30617674hg38UCSC Ensembl
chr10:30906603..30906603hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358700
Samples
Known GenesLYZL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967010
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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