A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624544



Internal ID21572849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50076816..50076816hg38UCSC Ensembl
chr10:51836576..51836576hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070806
SamplesHG03125
Known GenesFAM21A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624544
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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