A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462192



Internal ID21119745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:84881124..84881830hg38UCSC Ensembl
chr12:85274903..85275609hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005225
Samples
Known GenesSLC6A15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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