A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530592



Internal ID20903953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3689483..3694092hg38UCSC Ensembl
chr19:3689481..3694090hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384610
hg194610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198073
Samples
Known GenesPIP5K1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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