A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622449



Internal ID6662619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15604353..15766604hg38UCSC Ensembl
chr10:15646352..15808603hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38162252
hg19162252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv98e214
Supporting Variantsessv13704450, essv13704449
SamplesHG02756, HG03446
Known GenesITGA8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622449
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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