A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389261



Internal ID21046814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:27091471..27136915hg38UCSC Ensembl
chr5:27091578..27137022hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3845445
hg1945445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129903
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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