A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3443044



Internal ID15289997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114253163..114253622hg38UCSC Ensembl
Innerchr10:114253163..114253622hg38UCSC Ensembl
Outerchr10:114253009..114253898hg38UCSC Ensembl
chr10:116012922..116013381hg19UCSC Ensembl
Innerchr10:116012922..116013381hg19UCSC Ensembl
Outerchr10:116012768..116013657hg19UCSC Ensembl
chr10:116002912..116003371hg18UCSC Ensembl
Innerchr10:116002912..116003371hg18UCSC Ensembl
Outerchr10:116002758..116003647hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38460
hg19460
hg18460
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8651770
SamplesNA19240
Known GenesVWA2
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3443044
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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