A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460248



Internal ID21117801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15113593..15113987hg38UCSC Ensembl
chr12:15266527..15266921hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999582
Samples
Known GenesRERG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460248
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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