A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8701266



Internal ID13642185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89301839..89301839hg38UCSC Ensembl
Innerchr10:89301838..89301840hg38UCSC Ensembl
Outerchr10:89301789..89301889hg38UCSC Ensembl
chr10:91061596..91061596hg19UCSC Ensembl
Innerchr10:91061595..91061597hg19UCSC Ensembl
Outerchr10:91061546..91061646hg19UCSC Ensembl
chr10:91051576..91051576hg18UCSC Ensembl
Innerchr10:91051577..91051575hg18UCSC Ensembl
Outerchr10:91051526..91051626hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3879
hg1979
hg1879
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3431372
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8701266
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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