A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586860



Internal ID6972031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96254307..96260963hg38UCSC Ensembl
Innerchr1:96254307..96260963hg38UCSC Ensembl
Outerchr1:96254141..96261101hg38UCSC Ensembl
chr1:96719863..96726519hg19UCSC Ensembl
Innerchr1:96719863..96726519hg19UCSC Ensembl
Outerchr1:96719697..96726657hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg386657
hg196657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10025012
SamplesHG01079
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586860
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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