A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3444944



Internal ID14945210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97977506..97977524hg38UCSC Ensembl
Innerchr10:97977506..97977522hg38UCSC Ensembl
Outerchr10:97977488..97977542hg38UCSC Ensembl
chr10:99737263..99737281hg19UCSC Ensembl
Innerchr10:99737263..99737279hg19UCSC Ensembl
Outerchr10:99737245..99737299hg19UCSC Ensembl
chr10:99727253..99727271hg18UCSC Ensembl
Innerchr10:99727269..99727253hg18UCSC Ensembl
Outerchr10:99727235..99727289hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8949961, essv8949963, essv8949965, essv8949959, essv8949964, essv8949962, essv8949960
SamplesNA18861, NA18520, NA19114, NA18505, NA18912, NA18508, NA18853
Known GenesCRTAC1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3444944
Frequency
Sample Size185
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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