A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611697



Internal ID20984768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149134898..149160645hg38UCSC Ensembl
chr6:149456034..149481781hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3825748
hg1925748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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