A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897489



Internal ID22672593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44213339..44213489hg38UCSC Ensembl
chr6:44181076..44181226hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897489
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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