A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7746655



Internal ID14900379
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 StatusS
Merged Variantsesv3307179
Supporting Variants
SamplesNA19138
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7746655
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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