A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3332136



Internal ID14832410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104678170..104678189hg38UCSC Ensembl
Innerchr10:104678166..104678193hg38UCSC Ensembl
Outerchr10:104678147..104678212hg38UCSC Ensembl
chr10:106437928..106437947hg19UCSC Ensembl
Innerchr10:106437924..106437951hg19UCSC Ensembl
Outerchr10:106437905..106437970hg19UCSC Ensembl
chr10:106427918..106427937hg18UCSC Ensembl
Innerchr10:106427941..106427914hg18UCSC Ensembl
Outerchr10:106427895..106427960hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9649180
SamplesNA07346
Known GenesSORCS3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3332136
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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