A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622346



Internal ID7009205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11805142..11860059hg38UCSC Ensembl
Innerchr10:11805292..11859909hg38UCSC Ensembl
Outerchr10:11804992..11860209hg38UCSC Ensembl
chr10:11847141..11902058hg19UCSC Ensembl
Innerchr10:11847291..11901908hg19UCSC Ensembl
Outerchr10:11846991..11902208hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3854918
hg1954918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13696001, essv13696000
SamplesHG03803, NA18535
Known GenesPROSER2, PROSER2-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622346
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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