A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642347



Internal ID21590652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166997813..166997813hg38UCSC Ensembl
chr6:167411301..167411301hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381454
hg191454
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140011
SamplesHG00731
Known GenesMIR3939
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642347
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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