A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623863



Internal ID6664030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76202051..76206290hg38UCSC Ensembl
chr10:77961809..77966048hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg384240
hg194240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13864479, essv13864483, essv13864480, essv13864482, essv13864481
SamplesHG03985, HG00743, HG03836, HG01600, HG02442
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623863
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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