A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7843425



Internal ID13622466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5639727..5639727hg38UCSC Ensembl
chr10:5681690..5681690hg19UCSC Ensembl
chr10:5721696..5721696hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3865
hg1965
hg1865
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3310522
Supporting Variants
SamplesNA12878
Known GenesASB13
MethodSequencing
AnalysisCortex de-novo
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7843425
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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