A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622394



Internal ID7009253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13010910..13018998hg38UCSC Ensembl
Innerchr10:13010910..13018998hg38UCSC Ensembl
Outerchr10:13010661..13019227hg38UCSC Ensembl
chr10:13052910..13060998hg19UCSC Ensembl
Innerchr10:13052910..13060998hg19UCSC Ensembl
Outerchr10:13052661..13061227hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg388089
hg198089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13697861, essv13697860, essv13697863, essv13697862, essv13697864
SamplesHG00138, HG02490, HG02736, HG00708, NA07056
Known GenesCCDC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622394
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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