A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585485



Internal ID6625803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23581893..23583185hg38UCSC Ensembl
Innerchr1:23581895..23583183hg38UCSC Ensembl
Outerchr1:23581891..23583187hg38UCSC Ensembl
chr1:23908383..23909675hg19UCSC Ensembl
Innerchr1:23908385..23909673hg19UCSC Ensembl
Outerchr1:23908381..23909677hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381293
hg191293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9889485, essv9889486, essv9889489, essv9889487, essv9889488
SamplesHG03773, HG03015, HG03786, HG02787, HG02725
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585485
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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