A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910047



Internal ID22685257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168940100..168940175hg38UCSC Ensembl
chr6:169340195..169340270hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910047
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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