A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11543896



Internal ID6138737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100733354..100736632hg38UCSC Ensembl
Innerchr4:100733354..100736632hg38UCSC Ensembl
Outerchr4:100733116..100736895hg38UCSC Ensembl
chr4:101654511..101657789hg19UCSC Ensembl
Innerchr4:101654511..101657789hg19UCSC Ensembl
Outerchr4:101654273..101658052hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg383279
hg193279
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601581
Supporting Variants
SamplesNA19676
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11543896
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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