A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891802



Internal ID22666844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42160965..42162189hg38UCSC Ensembl
chr6:42128703..42129927hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381225
hg191225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433810
Samples
Known GenesGUCA1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891802
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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