A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643960



Internal ID6684029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22602151..22650770hg38UCSC Ensembl
chr19:22784953..22833572hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3848620
hg1948620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16013685
SamplesHG02391
Known GenesLOC100996349, LOC440518, ZNF492
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643960
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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