A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587818



Internal ID6975242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165970357..165991146hg38UCSC Ensembl
Innerchr1:165970357..165991146hg38UCSC Ensembl
Outerchr1:165969857..165991646hg38UCSC Ensembl
chr1:165939594..165960383hg19UCSC Ensembl
Innerchr1:165939594..165960383hg19UCSC Ensembl
Outerchr1:165939094..165960883hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3820790
hg1920790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10180467
SamplesHG03378
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587818
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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