A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597344



Internal ID6984572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109234688..109247670hg38UCSC Ensembl
Innerchr3:109235188..109247170hg38UCSC Ensembl
Outerchr3:109233688..109248670hg38UCSC Ensembl
chr3:108953535..108966517hg19UCSC Ensembl
Innerchr3:108954035..108966017hg19UCSC Ensembl
Outerchr3:108952535..108967517hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3812983
hg1912983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11097418
SamplesHG03007
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597344
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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