A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13855089



Internal ID1496294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69471214..69478253hg38UCSC Ensembl
Innerchr10:69471364..69478103hg38UCSC Ensembl
Outerchr10:69471064..69478403hg38UCSC Ensembl
chr10:71230970..71238009hg19UCSC Ensembl
Innerchr10:71231120..71237859hg19UCSC Ensembl
Outerchr10:71230820..71238159hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg387040
hg197040
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623746
Supporting Variants
SamplesHG01375
Known GenesTSPAN15
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13855089
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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