A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586652



Internal ID6974170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:83732126..83735063hg38UCSC Ensembl
Innerchr1:83732126..83735063hg38UCSC Ensembl
Outerchr1:83731950..83735226hg38UCSC Ensembl
chr1:84197809..84200746hg19UCSC Ensembl
Innerchr1:84197809..84200746hg19UCSC Ensembl
Outerchr1:84197633..84200909hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382938
hg192938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9996832
SamplesHG00692
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586652
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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