A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600487



Internal ID6987530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51977442..51988127hg38UCSC Ensembl
Innerchr4:51977442..51988127hg38UCSC Ensembl
Outerchr4:51976942..51988627hg38UCSC Ensembl
chr4:52843608..52854293hg19UCSC Ensembl
Innerchr4:52843608..52854293hg19UCSC Ensembl
Outerchr4:52843108..52854793hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3810686
hg1910686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11430701
SamplesHG02019
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600487
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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