A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470904



Internal ID21128457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:44491065..44491774hg38UCSC Ensembl
chr12:44884848..44885557hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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