A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414608



Internal ID21072161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42080632..42082518hg38UCSC Ensembl
chr6:42048370..42050256hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381887
hg191887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143359
Samples
Known GenesTAF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414608
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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