A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13913812



Internal ID5652219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102775660..102781271hg38UCSC Ensembl
Innerchr10:102775660..102781271hg38UCSC Ensembl
Outerchr10:102775593..102781344hg38UCSC Ensembl
chr10:104535417..104541028hg19UCSC Ensembl
Innerchr10:104535417..104541028hg19UCSC Ensembl
Outerchr10:104535350..104541101hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385612
hg195612
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624401
Supporting Variants
SamplesNA19067
Known GenesWBP1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13913812
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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