A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455876



Internal ID21113429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:23311701..23313500hg38UCSC Ensembl
chr12:23464635..23466434hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1443n223
Supporting Variantsnssv17998408
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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