A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597805



Internal ID6984943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131796107..131803916hg38UCSC Ensembl
Innerchr3:131796122..131803902hg38UCSC Ensembl
Outerchr3:131796093..131803931hg38UCSC Ensembl
chr3:131514951..131522760hg19UCSC Ensembl
Innerchr3:131514966..131522746hg19UCSC Ensembl
Outerchr3:131514937..131522775hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg387810
hg197810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11152001
SamplesHG03616
Known GenesCPNE4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597805
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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