A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585496



Internal ID6973019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24041192..24041975hg38UCSC Ensembl
Innerchr1:24041229..24041939hg38UCSC Ensembl
Outerchr1:24041156..24042012hg38UCSC Ensembl
chr1:24367682..24368465hg19UCSC Ensembl
Innerchr1:24367719..24368429hg19UCSC Ensembl
Outerchr1:24367646..24368502hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38784
hg19784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9890117, essv9890123, essv9890115, essv9890122, essv9890118, essv9890121, essv9890119, essv9890116, essv9890120
SamplesHG01438, NA20508, HG03717, HG01953, HG00232, NA20524, HG01494, NA11892, HG01695
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585496
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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