A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390689



Internal ID21048242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170064115..170064570hg38UCSC Ensembl
chr4:170985266..170985721hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115734
Samples
Known GenesAADAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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