A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458815



Internal ID21116368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:84878780..84879842hg38UCSC Ensembl
chr12:85272559..85273621hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg381063
hg191063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005224
Samples
Known GenesSLC6A15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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