A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586645



Internal ID6974163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:83473259..83489672hg38UCSC Ensembl
Innerchr1:83473259..83489672hg38UCSC Ensembl
Outerchr1:83472759..83490172hg38UCSC Ensembl
chr1:83938942..83955355hg19UCSC Ensembl
Innerchr1:83938942..83955355hg19UCSC Ensembl
Outerchr1:83938442..83955855hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3816414
hg1916414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9996333
SamplesNA19316
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586645
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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