A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622164



Internal ID7009023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3099237..3125437hg38UCSC Ensembl
chr10:3141429..3167629hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3826201
hg1926201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13678916, essv13678919, essv13678915, essv13678923, essv13678917, essv13678922, essv13678921, essv13678920, essv13678918
SamplesHG00626, HG00634, HG00610, HG00629, HG00266, HG00596, HG00404, NA12272, HG00628
Known GenesPFKP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622164
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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