A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11097385



Internal ID3757368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108891660..108931381hg38UCSC Ensembl
chr3:108610507..108650228hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3839722
hg1939722
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597336
Supporting Variants
SamplesHG03388
Known GenesGUCA1C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11097385
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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