A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3445912



Internal ID15292862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16694261..16694317hg38UCSC Ensembl
Innerchr3:16694273..16694302hg38UCSC Ensembl
Outerchr3:16694217..16694361hg38UCSC Ensembl
chr3:16735768..16735824hg19UCSC Ensembl
Innerchr3:16735780..16735809hg19UCSC Ensembl
Outerchr3:16735724..16735868hg19UCSC Ensembl
chr3:16710772..16710828hg18UCSC Ensembl
Innerchr3:16710813..16710784hg18UCSC Ensembl
Outerchr3:16710728..16710872hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38158
hg19158
hg18158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8912154, essv8912153
SamplesNA18504, NA18870
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3445912
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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