A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631220



Internal ID21579525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169771709..169771709hg38UCSC Ensembl
chr6:170171805..170171805hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141036
SamplesNA19983
Known GenesERMARD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631220
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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