A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644896



Internal ID6684959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57176512..57202860hg38UCSC Ensembl
chr19:57687880..57714228hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3826349
hg1926349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16107120
SamplesNA19019
Known GenesZNF264
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644896
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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