A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624662



Internal ID6664825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116669693..116679763hg38UCSC Ensembl
chr10:118429204..118439274hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3810071
hg1910071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946410, essv13946409
SamplesHG01412, HG01747
Known GenesC10orf82, HSPA12A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624662
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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