A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401680



Internal ID21059233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77466601..77467800hg38UCSC Ensembl
chr5:76762426..76763625hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135126
Samples
Known GenesWDR41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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