A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13710259



Internal ID5965276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18805063..18979875hg38UCSC Ensembl
chr10:19093992..19268804hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38174813
hg19174813
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622519
Supporting Variants
SamplesNA19378
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13710259
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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