A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13977653



Internal ID6010788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131446890..131640975hg38UCSC Ensembl
chr10:133245153..133473311hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38194086
hg19228159
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624960
Supporting Variants
SamplesNA19428
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13977653
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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