A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626934



Internal ID21575239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12401066..12401066hg38UCSC Ensembl
chr10:12443065..12443065hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067620
SamplesHG03371
Known GenesCAMK1D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626934
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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