A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475200



Internal ID21132753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:61392601..61439200hg38UCSC Ensembl
chr12:61786382..61832981hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3846600
hg1946600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475200
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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