A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622951



Internal ID7009809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37194692..37451861hg38UCSC Ensembl
chr10:37483620..37740789hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38257170
hg19257170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13756786
SamplesHG02697
Known GenesANKRD30A, LINC00993
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622951
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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