A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466994



Internal ID21124547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62373004..62373678hg38UCSC Ensembl
chr12:62766785..62767459hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002438
Samples
Known GenesUSP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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