A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449990



Internal ID21107543
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 StatusM
Merged Variants
Supporting Variantsnssv18188245
Samples
Known GenesCAMK1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449990
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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