A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602409



Internal ID20975480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141510930..141511366hg38UCSC Ensembl
chr6:141832067..141832503hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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