A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529226



Internal ID20902587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14539014..14540191hg38UCSC Ensembl
chr19:14649826..14651003hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381178
hg191178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197405
Samples
Known GenesTECR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529226
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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