A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13903876



Internal ID3905694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95309786..95356777hg38UCSC Ensembl
chr10:97069543..97116534hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3846992
hg1946992
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624276
Supporting Variants
SamplesHG03378
Known GenesSORBS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13903876
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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