A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611486



Internal ID20984557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141405775..141436595hg38UCSC Ensembl
chr6:141726912..141757732hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3830821
hg1930821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611486
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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