A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3381443



Internal ID14881718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1575046..1575046hg38UCSC Ensembl
Innerchr10:1575045..1575047hg38UCSC Ensembl
Outerchr10:1574996..1575096hg38UCSC Ensembl
chr10:1617241..1617241hg19UCSC Ensembl
Innerchr10:1617240..1617242hg19UCSC Ensembl
Outerchr10:1617191..1617291hg19UCSC Ensembl
chr10:1607241..1607241hg18UCSC Ensembl
Innerchr10:1607242..1607240hg18UCSC Ensembl
Outerchr10:1607191..1607291hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8701259
SamplesNA12878
Known GenesADARB2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3381443
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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