A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601563



Internal ID6988600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99997396..99998136hg38UCSC Ensembl
Innerchr4:99997406..99998126hg38UCSC Ensembl
Outerchr4:99997386..99998146hg38UCSC Ensembl
chr4:100918553..100919293hg19UCSC Ensembl
Innerchr4:100918563..100919283hg19UCSC Ensembl
Outerchr4:100918543..100919303hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11543449, essv11543448, essv11543440, essv11543446, essv11543441, essv11543451, essv11543445, essv11543443, essv11543444, essv11543450, essv11543447, essv11543438, essv11543439, essv11543442
SamplesHG00102, HG00242, HG00100, HG01531, NA20805, HG00150, NA11918, NA20775, HG00740, HG00246, HG00258, HG01086, HG01776, NA11832
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601563
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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