A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595361



Internal ID6982679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14070505..14072911hg38UCSC Ensembl
Innerchr3:14070517..14072900hg38UCSC Ensembl
Outerchr3:14070494..14072923hg38UCSC Ensembl
chr3:14112005..14114411hg19UCSC Ensembl
Innerchr3:14112017..14114400hg19UCSC Ensembl
Outerchr3:14111994..14114423hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg382407
hg192407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10932038
SamplesNA20896
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595361
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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