A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13889842



Internal ID3951615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88089917..88116723hg38UCSC Ensembl
Innerchr10:88089958..88116683hg38UCSC Ensembl
Outerchr10:88089877..88116764hg38UCSC Ensembl
chr10:89849674..89876480hg19UCSC Ensembl
Innerchr10:89849715..89876440hg19UCSC Ensembl
Outerchr10:89849634..89876521hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3826807
hg1926807
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624121
Supporting Variants
SamplesHG03603
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13889842
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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