A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891263



Internal ID22666298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7272862..7273506hg38UCSC Ensembl
chr6:7273095..7273739hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1741n209
Supporting Variantsnssv17434720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891263
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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