A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467221



Internal ID21124774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2860727..2870742hg38UCSC Ensembl
chr12:2969893..2979908hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3810016
hg1910016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998501
Samples
Known GenesFOXM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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