A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597074



Internal ID6637344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96614806..96628736hg38UCSC Ensembl
Innerchr3:96614829..96628714hg38UCSC Ensembl
Outerchr3:96614784..96628759hg38UCSC Ensembl
chr3:96333650..96347580hg19UCSC Ensembl
Innerchr3:96333673..96347558hg19UCSC Ensembl
Outerchr3:96333628..96347603hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3813931
hg1913931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv912e214
Supporting Variantsessv11074005
SamplesHG03397
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597074
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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