A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910201



Internal ID22685411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17828147..17832657hg38UCSC Ensembl
chr10:17870146..17874656hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg384511
hg194511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365197
Samples
Known GenesMRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910201
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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