A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471796



Internal ID21129349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54835429..54836103hg38UCSC Ensembl
chr12:55229213..55229887hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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