A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601671



Internal ID6988707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105997710..106009934hg38UCSC Ensembl
Innerchr4:105997734..106009911hg38UCSC Ensembl
Outerchr4:105997687..106009958hg38UCSC Ensembl
chr4:106918867..106931091hg19UCSC Ensembl
Innerchr4:106918891..106931068hg19UCSC Ensembl
Outerchr4:106918844..106931115hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3812225
hg1912225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11554281
SamplesHG03808
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601671
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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