A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467988



Internal ID21125541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53470101..53471400hg38UCSC Ensembl
chr12:53863885..53865184hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001458
Samples
Known GenesPCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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