A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417611



Internal ID21075164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139939001..139939900hg38UCSC Ensembl
chr8:140951284..140952183hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167214
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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