A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900567



Internal ID22675710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108289524..108293815hg38UCSC Ensembl
chr6:108610728..108615019hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384292
hg194292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1799n209
Supporting Variantsnssv17420484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900567
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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