A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406624



Internal ID21064177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1553725..1555878hg38UCSC Ensembl
chr6:1553960..1556113hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406624
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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