A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585209



Internal ID6625528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10976983..10978065hg38UCSC Ensembl
Innerchr1:10976983..10978065hg38UCSC Ensembl
Outerchr1:10976790..10978296hg38UCSC Ensembl
chr1:11037040..11038122hg19UCSC Ensembl
Innerchr1:11037040..11038122hg19UCSC Ensembl
Outerchr1:11036847..11038353hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9853353
SamplesHG00159
Known GenesC1orf127
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585209
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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