A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv98e214



Internal ID20121521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15603295..15766604hg38UCSC Ensembl
chr10:15645294..15808603hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38163310
hg19163310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3622449, esv3622448
SamplesHG02756, HG03446, NA20276
Known GenesITGA8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv98e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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