A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644229



Internal ID6684297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35210814..35235012hg38UCSC Ensembl
chr19:35701717..35725915hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3824199
hg1924199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16045661, essv16045663, essv16045662
SamplesNA19031, NA19331, NA19334
Known GenesFAM187B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644229
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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