A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067620



Internal ID21473888
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 StatusS
Merged Variantsnsv5626934
Supporting Variants
SamplesHG03371
Known GenesCAMK1D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067620
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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