A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290277



Internal ID20499495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12401020..12401020hg38UCSC Ensembl
chr10:12443019..12443019hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765103
Supporting Variants
Samples
Known GenesCAMK1D
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290277
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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