A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11097277



Internal ID1099093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108759794..108933305hg38UCSC Ensembl
chr3:108478641..108652152hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38173512
hg19173512
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597329
Supporting Variants
SamplesHG03388
Known GenesGUCA1C, TRAT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11097277
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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