A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461650



Internal ID21119203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101156318..101156991hg38UCSC Ensembl
chr12:101550096..101550769hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38674
hg19674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996684
Samples
Known GenesSLC5A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461650
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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