A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13866675



Internal ID6669272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78578504..78580108hg38UCSC Ensembl
Innerchr10:78578512..78580101hg38UCSC Ensembl
Outerchr10:78578497..78580116hg38UCSC Ensembl
chr10:80338261..80339865hg19UCSC Ensembl
Innerchr10:80338269..80339858hg19UCSC Ensembl
Outerchr10:80338254..80339873hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381605
hg191605
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623894
Supporting Variants
SamplesNA20809
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13866675
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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