A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7731067



Internal ID13376012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86524709..86524812hg38UCSC Ensembl
Innerchr10:86524760..86524761hg38UCSC Ensembl
Outerchr10:86524609..86524912hg38UCSC Ensembl
chr10:88284466..88284569hg19UCSC Ensembl
Innerchr10:88284517..88284518hg19UCSC Ensembl
Outerchr10:88284366..88284669hg19UCSC Ensembl
chr10:88274446..88274549hg18UCSC Ensembl
Innerchr10:88274498..88274497hg18UCSC Ensembl
Outerchr10:88274346..88274649hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38104
hg19104
hg18104
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302624
Supporting Variants
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7731067
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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