A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365632



Internal ID21023185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68115412..68177920hg38UCSC Ensembl
chr3:68164562..68227070hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3862509
hg1962509
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213011
Samples
Known GenesFAM19A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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