A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907638



Internal ID22682848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72274352..72274491hg38UCSC Ensembl
chr10:74034110..74034249hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363077
Samples
Known GenesDDIT4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907638
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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