A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415690



Internal ID21073243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39120902..39123315hg38UCSC Ensembl
chr8:38978421..38980834hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg382414
hg192414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169004
Samples
Known GenesADAM32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415690
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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