A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188245



Internal ID20755285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12735277..12746186hg38UCSC Ensembl
chr10:12777276..12788185hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3810910
hg1910910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449990
Supporting Variants
Samples
Known GenesCAMK1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188245
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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