A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597249



Internal ID6972183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104355648..104419773hg38UCSC Ensembl
Innerchr3:104356148..104419273hg38UCSC Ensembl
Outerchr3:104354648..104420773hg38UCSC Ensembl
chr3:104074492..104138617hg19UCSC Ensembl
Innerchr3:104074992..104138117hg19UCSC Ensembl
Outerchr3:104073492..104139617hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3864126
hg1964126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11092047
SamplesHG02442
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597249
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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