A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635931



Internal ID21584236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46824894..46824894hg38UCSC Ensembl
chr6:46792631..46792631hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154248
SamplesHG03486
Known GenesMEP1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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