A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586257



Internal ID6973777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64259250..64263379hg38UCSC Ensembl
Innerchr1:64259300..64263329hg38UCSC Ensembl
Outerchr1:64259200..64263429hg38UCSC Ensembl
chr1:64724933..64729062hg19UCSC Ensembl
Innerchr1:64724983..64729012hg19UCSC Ensembl
Outerchr1:64724883..64729112hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg384130
hg194130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9951282
SamplesHG03616
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586257
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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