A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376779



Internal ID21034332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170061608..170062165hg38UCSC Ensembl
chr4:170982759..170983316hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115733
Samples
Known GenesAADAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376779
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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