A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425307



Internal ID22483177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169692358..169693261hg38UCSC Ensembl
chr6:170092454..170093357hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38904
hg19904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916847
Supporting Variants
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425307
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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