A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925202



Internal ID22700429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166930725..166930906hg38UCSC Ensembl
chr6:167344213..167344394hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422768
Samples
Known GenesRNASET2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925202
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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