A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633386



Internal ID7020195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102946677..102951194hg38UCSC Ensembl
Innerchr13:102946680..102951191hg38UCSC Ensembl
Outerchr13:102946674..102951197hg38UCSC Ensembl
chr13:103599027..103603544hg19UCSC Ensembl
Innerchr13:103599030..103603541hg19UCSC Ensembl
Outerchr13:103599024..103603547hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg384518
hg194518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14881015, essv14881018, essv14881014, essv14881016, essv14881017
SamplesNA18502, HG03558, NA19201, NA19391, NA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633386
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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