A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603406



Internal ID6990437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181296087..181298083hg38UCSC Ensembl
Innerchr4:181296116..181298054hg38UCSC Ensembl
Outerchr4:181296058..181298112hg38UCSC Ensembl
chr4:182217240..182219236hg19UCSC Ensembl
Innerchr4:182217269..182219207hg19UCSC Ensembl
Outerchr4:182217211..182219265hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg381997
hg191997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11730306, essv11730309, essv11730304, essv11730312, essv11730310, essv11730305, essv11730307, essv11730308, essv11730311
SamplesHG02811, HG02571, NA19209, NA18908, HG03476, HG03354, HG02484, HG03439, NA19153
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603406
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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