A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13945113



Internal ID4344866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115952102..115952488hg38UCSC Ensembl
Innerchr10:115952102..115952488hg38UCSC Ensembl
Outerchr10:115952102..115952488hg38UCSC Ensembl
chr10:117711613..117711999hg19UCSC Ensembl
Innerchr10:117711613..117711999hg19UCSC Ensembl
Outerchr10:117711613..117711999hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624647
Supporting Variants
SamplesHG03885
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13945113
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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