A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8947649



Internal ID13896523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26751419..26751433hg38UCSC Ensembl
Innerchr10:26751415..26751435hg38UCSC Ensembl
Outerchr10:26751401..26751451hg38UCSC Ensembl
chr10:27040348..27040362hg19UCSC Ensembl
Innerchr10:27040344..27040364hg19UCSC Ensembl
Outerchr10:27040330..27040380hg19UCSC Ensembl
chr10:27080354..27080368hg18UCSC Ensembl
Innerchr10:27080370..27080350hg18UCSC Ensembl
Outerchr10:27080336..27080386hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3406827
Supporting Variants
SamplesNA18582
Known GenesABI1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8947649
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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