A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460679



Internal ID21118232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15171701..15173900hg38UCSC Ensembl
chr12:15324635..15326834hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999584
Samples
Known GenesRERG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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