A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307179



Internal ID15154127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23580163..23580164hg38UCSC Ensembl
Innerchr10:23580134..23580193hg38UCSC Ensembl
Outerchr10:23580133..23580194hg38UCSC Ensembl
chr10:23869092..23869093hg19UCSC Ensembl
Innerchr10:23869063..23869122hg19UCSC Ensembl
Outerchr10:23869062..23869123hg19UCSC Ensembl
chr10:23909098..23909099hg18UCSC Ensembl
Innerchr10:23909128..23909069hg18UCSC Ensembl
Outerchr10:23909068..23909129hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38243
hg19243
hg18243
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7743918, essv7742462, essv7763079, essv7746655, essv7756170
SamplesNA18870, NA19138, NA18520, NA18907, NA18511
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307179
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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