A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7838797



Internal ID15007558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34323324..34323325hg38UCSC Ensembl
Innerchr10:34323278..34323371hg38UCSC Ensembl
Outerchr10:34323277..34323372hg38UCSC Ensembl
chr10:34612252..34612253hg19UCSC Ensembl
Innerchr10:34612206..34612299hg19UCSC Ensembl
Outerchr10:34612205..34612300hg19UCSC Ensembl
chr10:34652258..34652259hg18UCSC Ensembl
Innerchr10:34652305..34652212hg18UCSC Ensembl
Outerchr10:34652211..34652306hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3886
hg1986
hg1886
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308910
Supporting Variants
SamplesNA19238
Known GenesPARD3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7838797
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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