A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622772



Internal ID6662941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29423054..29427511hg38UCSC Ensembl
Innerchr10:29423064..29427502hg38UCSC Ensembl
Outerchr10:29423045..29427521hg38UCSC Ensembl
chr10:29711983..29716440hg19UCSC Ensembl
Innerchr10:29711993..29716431hg19UCSC Ensembl
Outerchr10:29711974..29716450hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg384458
hg194458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13742727
SamplesHG03060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622772
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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