A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904477



Internal ID22679654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158893414..158898025hg38UCSC Ensembl
chr6:159314446..159319057hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384612
hg194612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1804n209
Supporting Variantsnssv17412193
Samples
Known GenesC6orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904477
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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