A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326534



Internal ID20859670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17073123..17088313hg38UCSC Ensembl
chr1:17399618..17414808hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3815191
hg1915191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201668
Samples
Known GenesPADI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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