A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622229



Internal ID7009088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5423434..5424872hg38UCSC Ensembl
Innerchr10:5423484..5424822hg38UCSC Ensembl
Outerchr10:5423374..5424932hg38UCSC Ensembl
chr10:5465397..5466835hg19UCSC Ensembl
Innerchr10:5465447..5466785hg19UCSC Ensembl
Outerchr10:5465337..5466895hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381439
hg191439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13685575, essv13685576, essv13685573, essv13685577, essv13685572, essv13685574
SamplesHG01855, HG02375, HG02185, HG01811, HG00623, HG02406
Known GenesNET1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622229
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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