A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604535



Internal ID20977606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121266510..121272707hg38UCSC Ensembl
chr6:121587656..121593853hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg386198
hg196198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137524
Samples
Known GenesTBC1D32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604535
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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