A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462212



Internal ID21119765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14827689..14835824hg38UCSC Ensembl
chr12:14980623..14988758hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg388136
hg198136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999552
Samples
Known GenesART4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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