A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919410



Internal ID22694632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28598344..28598469hg38UCSC Ensembl
chr10:28887273..28887398hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352738
Samples
Known GenesWAC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919410
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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