A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8694692



Internal ID13640111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181461545..181478243hg38UCSC Ensembl
Innerchr5:181462545..181477243hg38UCSC Ensembl
Outerchr5:181460545..181478259hg38UCSC Ensembl
chr5:180888546..180905244hg19UCSC Ensembl
Innerchr5:180889546..180904244hg19UCSC Ensembl
Outerchr5:180887546..180905260hg19UCSC Ensembl
chr5:180821152..180837850hg18UCSC Ensembl
Innerchr5:180822152..180836850hg18UCSC Ensembl
Outerchr5:180820152..180838850hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3816699
hg1916699
hg1816699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3376773
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8694692
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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