A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623946



Internal ID7010802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80133465..80175734hg38UCSC Ensembl
chr10:81893221..81935490hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3842270
hg1942270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13870325, essv13870326, essv13870327
SamplesHG01133, HG00349, NA12718
Known GenesANXA11, PLAC9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623946
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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