A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868370



Internal ID22643305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104948743..104949729hg38UCSC Ensembl
chr1:105491365..105492351hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868370
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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