A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893416



Internal ID22668476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52994562..52995774hg38UCSC Ensembl
chr6:52859360..52860572hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg381213
hg191213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449057
Samples
Known GenesGSTA4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893416
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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