A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585359



Internal ID6625678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17077448..17111045hg38UCSC Ensembl
chr1:17403943..17437540hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3833598
hg1933598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9874572
SamplesHG01935
Known GenesPADI2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585359
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer