A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459158



Internal ID21116711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4181380..4182396hg38UCSC Ensembl
chr12:4290546..4291562hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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