A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424617



Internal ID21082170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88603415..88701466hg38UCSC Ensembl
chr8:89615644..89713695hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3898052
hg1998052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424617
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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