A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895513



Internal ID22670597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8432262..8434991hg38UCSC Ensembl
chr6:8432495..8435224hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg382730
hg192730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438910
Samples
Known GenesSLC35B3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895513
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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