A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401858



Internal ID21059411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32968101..32969600hg38UCSC Ensembl
chr6:32935878..32937377hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142242
Samples
Known GenesBRD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401858
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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