A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465299



Internal ID21122852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6216606..6219169hg38UCSC Ensembl
chr12:6325772..6328335hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg382564
hg192564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002420
Samples
Known GenesCD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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