A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529929



Internal ID20903290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12639204..12649548hg38UCSC Ensembl
chr19:12750018..12760362hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3810345
hg1910345
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197354
Samples
Known GenesMAN2B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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