A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413033



Internal ID22470903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166162673..166162798hg38UCSC Ensembl
chr6:166576161..166576286hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924814
Supporting Variants
Samples
Known GenesT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413033
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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