A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581547



Internal ID21530047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116429650..116429968hg38UCSC Ensembl
chr6:116750813..116751131hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144035
SamplesHG00731
Known GenesDSE
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581547
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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