A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11684606



Internal ID6146808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166701863..166717167hg38UCSC Ensembl
Innerchr4:166701863..166717167hg38UCSC Ensembl
Outerchr4:166701363..166717667hg38UCSC Ensembl
chr4:167623014..167638318hg19UCSC Ensembl
Innerchr4:167623014..167638318hg19UCSC Ensembl
Outerchr4:167622514..167638818hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3815305
hg1915305
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603049
Supporting Variants
SamplesNA19681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11684606
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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