A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586996



Internal ID6974423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102607545..102641032hg38UCSC Ensembl
Innerchr1:102607545..102641032hg38UCSC Ensembl
Outerchr1:102607045..102641532hg38UCSC Ensembl
chr1:103073101..103106588hg19UCSC Ensembl
Innerchr1:103073101..103106588hg19UCSC Ensembl
Outerchr1:103072601..103107088hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3833488
hg1933488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10036519
SamplesHG01870
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586996
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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