A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622931



Internal ID7009789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36641768..36677382hg38UCSC Ensembl
chr10:36930696..36966310hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3835615
hg1935615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13756675
SamplesHG02697
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622931
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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