A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418805



Internal ID22476675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166256101..166256161hg38UCSC Ensembl
chr6:166669589..166669649hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922796
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418805
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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