A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460555



Internal ID21118108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2915657..2919005hg38UCSC Ensembl
chr12:3024823..3028171hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg383349
hg193349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998561
Samples
Known GenesTULP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460555
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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