A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603883



Internal ID20976954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108289479..108293877hg38UCSC Ensembl
chr6:108610683..108615081hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384399
hg194399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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