A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622960



Internal ID7009818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37442414..37747570hg38UCSC Ensembl
chr10:37731342..38036498hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38305157
hg19305157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13756807
SamplesHG02697
Known GenesMTRNR2L7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622960
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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