A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599768



Internal ID6986813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17034460..17038530hg38UCSC Ensembl
Innerchr4:17034543..17038480hg38UCSC Ensembl
Outerchr4:17034356..17038634hg38UCSC Ensembl
chr4:17036083..17040153hg19UCSC Ensembl
Innerchr4:17036166..17040103hg19UCSC Ensembl
Outerchr4:17035979..17040257hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg384071
hg194071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11360433, essv11360425, essv11360431, essv11360426, essv11360430, essv11360428, essv11360432, essv11360429, essv11360424, essv11360427
SamplesHG03096, HG03115, NA19197, HG03225, NA19247, HG03159, HG03294, HG03567, NA19108, NA19102
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599768
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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