A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611364



Internal ID20984435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144115196..144126838hg38UCSC Ensembl
chr6:144436333..144447975hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3811643
hg1911643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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