A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904340



Internal ID22679517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92821231..92905548hg38UCSC Ensembl
chr6:93530949..93615266hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3884318
hg1984318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904340
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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