A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9889488



Internal ID6514781
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585485
Supporting Variants
SamplesHG03773
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9889488
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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