A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585196



Internal ID6972720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10185208..10190887hg38UCSC Ensembl
Innerchr1:10185708..10190387hg38UCSC Ensembl
Outerchr1:10184208..10191887hg38UCSC Ensembl
chr1:10245266..10250945hg19UCSC Ensembl
Innerchr1:10245766..10250445hg19UCSC Ensembl
Outerchr1:10244266..10251945hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg385680
hg195680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9851644
SamplesHG02561
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585196
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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