A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13933961



Internal ID3935777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110252088..110255060hg38UCSC Ensembl
Innerchr10:110252088..110255060hg38UCSC Ensembl
Outerchr10:110251884..110255236hg38UCSC Ensembl
chr10:112011846..112014818hg19UCSC Ensembl
Innerchr10:112011846..112014818hg19UCSC Ensembl
Outerchr10:112011642..112014994hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382973
hg192973
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624538
Supporting Variants
SamplesNA19712
Known GenesMXI1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13933961
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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