A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622448



Internal ID6662618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15603295..15746399hg38UCSC Ensembl
chr10:15645294..15788398hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38143105
hg19143105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv98e214
Supporting Variantsessv13704446, essv13704447, essv13704448
SamplesHG02756, HG03446, NA20276
Known GenesITGA8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622448
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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