A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644253



Internal ID6684321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36321310..36347053hg38UCSC Ensembl
chr19:36812212..36837955hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3825744
hg1925744
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16048769, essv16048770
SamplesNA20796, HG01378
Known GenesLINC00665, ZFP14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644253
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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