A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427324



Internal ID22485194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158892891..158897616hg38UCSC Ensembl
chr6:159313923..159318648hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384726
hg194726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894344
Supporting Variants
Samples
Known GenesC6orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427324
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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