A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466393



Internal ID21123946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:84881421..84882067hg38UCSC Ensembl
chr12:85275200..85275846hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005226
Samples
Known GenesSLC6A15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466393
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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