A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612992



Internal ID20986063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151375820..151377785hg38UCSC Ensembl
chr6:151696955..151698920hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381966
hg191966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141485
Samples
Known GenesZBTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612992
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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