A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905477



Internal ID22680664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148865211..148869424hg38UCSC Ensembl
chr6:149186347..149190560hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384214
hg194214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428549
Samples
Known GenesUST
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905477
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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