A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415604



Internal ID21073157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98304139..98311027hg38UCSC Ensembl
chr8:99316367..99323255hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg386889
hg196889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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