A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16081560



Internal ID6025653
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644684
Supporting Variants
SamplesNA19435
Known GenesZNF432, ZNF616, ZNF841
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16081560
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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