A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623185



Internal ID6663353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45995694..46106028hg38UCSC Ensembl
chr10:51489794..51600128hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38110335
hg19110335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13799684, essv13799686, essv13799683, essv13799685
SamplesNA19435, HG03548, NA18868, NA19922
Known GenesMSMB, NCOA4, TIMM23
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623185
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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