A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585307



Internal ID6972832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15243149..15244748hg38UCSC Ensembl
Innerchr1:15243163..15244735hg38UCSC Ensembl
Outerchr1:15243136..15244762hg38UCSC Ensembl
chr1:15569645..15571244hg19UCSC Ensembl
Innerchr1:15569659..15571231hg19UCSC Ensembl
Outerchr1:15569632..15571258hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9863640
SamplesHG01860
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585307
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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