A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404147



Internal ID21061700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111309148..111309759hg38UCSC Ensembl
chr5:110644846..110645457hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124972
Samples
Known GenesCAMK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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