A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3306603



Internal ID15153551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176896933..176896934hg38UCSC Ensembl
Innerchr5:176896906..176896961hg38UCSC Ensembl
Outerchr5:176896905..176896962hg38UCSC Ensembl
chr5:176323934..176323935hg19UCSC Ensembl
Innerchr5:176323907..176323962hg19UCSC Ensembl
Outerchr5:176323906..176323963hg19UCSC Ensembl
chr5:176256540..176256541hg18UCSC Ensembl
Innerchr5:176256568..176256513hg18UCSC Ensembl
Outerchr5:176256512..176256569hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38235
hg19235
hg18235
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7759877, essv7762186, essv7760236, essv7754758, essv7741021, essv7763153, essv7758759, essv7750228
SamplesNA18861, NA18489, NA19172, NA19239, NA18907, NA18517, NA18501, NA19129
Known GenesHK3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3306603
Frequency
Sample Size185
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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