A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643571



Internal ID6683642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6896401..7019801hg38UCSC Ensembl
chr19:6896412..7019812hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38123401
hg19123401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15986860, essv15986859, essv15986861, essv15986858
SamplesNA20524, HG04195, HG01879, HG04186
Known GenesEMR1, EMR4P, FLJ25758
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643571
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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