A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377126



Internal ID21034679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26209683..26290985hg38UCSC Ensembl
chr5:26209792..26291094hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3881303
hg1981303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377126
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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