A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419903



Internal ID21077456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24498101..24498900hg38UCSC Ensembl
chr8:24355614..24356413hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167821
Samples
Known GenesADAM7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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