A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406778



Internal ID21064331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135449809..135451625hg38UCSC Ensembl
chr5:134785499..134787315hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127842
Samples
Known GenesTIFAB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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