A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390570



Internal ID21048123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87854336..87854801hg38UCSC Ensembl
chr4:88775488..88775953hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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