A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896837



Internal ID22671933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80408167..80409614hg38UCSC Ensembl
chr6:81117884..81119331hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381448
hg191448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896837
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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