A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9649180



Internal ID12708505
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 Flag1
Merged StatusS
Merged Variantsesv3332136
Supporting Variants
SamplesNA07346
Known GenesSORCS3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9649180
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer