A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644684



Internal ID7031438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52028467..52118719hg38UCSC Ensembl
chr19:52531720..52621972hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3890253
hg1990253
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16081560, essv16081559, essv16081558
SamplesNA19435, NA19430, NA11832
Known GenesZNF432, ZNF616, ZNF841
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644684
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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