A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403790



Internal ID21061343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103033311..103057209hg38UCSC Ensembl
chr5:102369015..102392913hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3823899
hg1923899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403790
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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