A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585517



Internal ID6973040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24983974..24984527hg38UCSC Ensembl
Innerchr1:24984024..24984477hg38UCSC Ensembl
Outerchr1:24983836..24984665hg38UCSC Ensembl
chr1:25310465..25311018hg19UCSC Ensembl
Innerchr1:25310515..25310968hg19UCSC Ensembl
Outerchr1:25310327..25311156hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9892207, essv9892208
SamplesNA19024, NA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585517
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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