A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587159



Internal ID6974586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109844542..109859614hg38UCSC Ensembl
Innerchr1:109844542..109859614hg38UCSC Ensembl
Outerchr1:109844042..109860114hg38UCSC Ensembl
chr1:110387164..110402236hg19UCSC Ensembl
Innerchr1:110387164..110402236hg19UCSC Ensembl
Outerchr1:110386664..110402736hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3815073
hg1915073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10061168
SamplesHG01396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587159
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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