A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468809



Internal ID21126362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48901842..48909259hg38UCSC Ensembl
chr12:49295625..49303042hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg387418
hg197418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178431
Samples
Known GenesCCDC65
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468809
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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