A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901852



Internal ID22677005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79239113..79239468hg38UCSC Ensembl
chr6:79948830..79949185hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901852
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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