A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456451



Internal ID21114004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40194201..40198400hg38UCSC Ensembl
chr12:40588003..40592202hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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