A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585191



Internal ID6972715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9915519..9920179hg38UCSC Ensembl
Innerchr1:9915519..9920179hg38UCSC Ensembl
Outerchr1:9915344..9920363hg38UCSC Ensembl
chr1:9975577..9980237hg19UCSC Ensembl
Innerchr1:9975577..9980237hg19UCSC Ensembl
Outerchr1:9975402..9980421hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384661
hg194661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9851625
SamplesHG00607
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585191
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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