A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469474



Internal ID21127027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25695059..25695514hg38UCSC Ensembl
chr12:25847993..25848448hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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