A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608706



Internal ID20981777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153563660..153724871hg38UCSC Ensembl
chr6:153884795..154046006hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38161212
hg19161212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141638
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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