A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412609



Internal ID21070162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33301425..33303193hg38UCSC Ensembl
chr6:33269202..33270970hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381769
hg191769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142831
Samples
Known GenesTAPBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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