A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978486



Internal ID20545526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12396540..12406592hg38UCSC Ensembl
chr10:12438539..12448591hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3810053
hg1910053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438308
Supporting Variants
Samples
Known GenesCAMK1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978486
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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