A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917860



Internal ID22693081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4719551..4740519hg38UCSC Ensembl
chr10:4761743..4782711hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3820969
hg1920969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366810
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917860
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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