A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430069



Internal ID21087622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90028301..90029300hg38UCSC Ensembl
chr8:91040529..91041528hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173680
Samples
Known GenesDECR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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