A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603527



Internal ID6990558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186309943..186312938hg38UCSC Ensembl
Innerchr4:186309943..186312938hg38UCSC Ensembl
Outerchr4:186309654..186313241hg38UCSC Ensembl
chr4:187231097..187234092hg19UCSC Ensembl
Innerchr4:187231097..187234092hg19UCSC Ensembl
Outerchr4:187230808..187234395hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg382996
hg192996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11746344, essv11746335, essv11746340, essv11746345, essv11746331, essv11746339, essv11746336, essv11746334, essv11746341, essv11746337, essv11746332, essv11746346, essv11746342, essv11746333, essv11746338, essv11746343
SamplesNA19394, NA18881, HG03298, HG02621, HG03168, NA19041, NA20340, HG02946, NA19247, HG02881, HG02979, HG02256, NA19144, HG02013, NA19146, HG03166
Known GenesF11-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603527
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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