A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13721444



Internal ID6535831
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622656
Supporting Variants
SamplesNA20585
Known GenesPRTFDC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13721444
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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