A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643861



Internal ID6683930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19916242..19962639hg38UCSC Ensembl
chr19:20027051..20073448hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3846398
hg1946398
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16006940
SamplesHG03472
Known GenesZNF93
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643861
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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