A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622656



Internal ID7009514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24856653..24857771hg38UCSC Ensembl
Innerchr10:24856662..24857762hg38UCSC Ensembl
Outerchr10:24856644..24857780hg38UCSC Ensembl
chr10:25145582..25146700hg19UCSC Ensembl
Innerchr10:25145591..25146691hg19UCSC Ensembl
Outerchr10:25145573..25146709hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381119
hg191119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13721444, essv13721442, essv13721443, essv13721441, essv13721445
SamplesNA20588, HG00103, NA19064, HG00373, NA20585
Known GenesPRTFDC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622656
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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