A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644738



Internal ID6684802
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16089191, essv16089187, essv16089190, essv16089186, essv16089188, essv16089189
SamplesHG02790, HG02685, NA20849, HG03636, HG03640, HG00566
Known GenesZNF160, ZNF415
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644738
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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