A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912267



Internal ID22687483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2264138..2264359hg38UCSC Ensembl
chr10:2306332..2306553hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912267
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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