A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435577



Internal ID21397579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86176025..86181514hg38UCSC Ensembl
chr8:87188254..87193743hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg385490
hg195490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750451
SamplesSMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435577
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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