A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401909



Internal ID21059462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80305798..80317158hg38UCSC Ensembl
chr5:79601617..79612977hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3811361
hg1911361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133483
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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