A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149090



Internal ID21495479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88907354..88907413hg38UCSC Ensembl
chr6:89617073..89617132hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569373
Supporting Variants
SamplesNA19238
Known GenesRNGTT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149090
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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