A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893084



Internal ID22668141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94028391..94498018hg38UCSC Ensembl
chr6:94738109..95207736hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38469628
hg19469628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438494
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893084
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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