A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924039



Internal ID22699266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4815524..4815987hg38UCSC Ensembl
chr10:4857716..4858179hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924039
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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