A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460352



Internal ID21117905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9926201..9927800hg38UCSC Ensembl
chr12:10078800..10080399hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006191
Samples
Known GenesCLEC2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460352
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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