A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587651



Internal ID6975073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157445550..157446122hg38UCSC Ensembl
Innerchr1:157445600..157446072hg38UCSC Ensembl
Outerchr1:157445500..157446172hg38UCSC Ensembl
chr1:157415340..157415912hg19UCSC Ensembl
Innerchr1:157415390..157415862hg19UCSC Ensembl
Outerchr1:157415290..157415962hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10155271
SamplesNA18987
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587651
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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