A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624604



Internal ID6664768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113582786..113669854hg38UCSC Ensembl
chr10:115342545..115429613hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3887069
hg1987069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13941208
SamplesHG01757
Known GenesHABP2, NRAP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624604
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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