A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601581



Internal ID6988618
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11543894, essv11543895, essv11543896
SamplesNA19654, HG02283, NA19676
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601581
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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