A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155644



Internal ID21457123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166636336..166636336hg38UCSC Ensembl
chr6:167049824..167049824hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640256
Supporting Variants
SamplesHG02587
Known GenesRPS6KA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155644
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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