A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16089189



Internal ID3982296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53096367..53124914hg38UCSC Ensembl
chr19:53599620..53628167hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3828548
hg1928548
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644738
Supporting Variants
SamplesHG03636
Known GenesZNF160, ZNF415
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16089189
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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