A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585591



Internal ID6625907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28752474..28753888hg38UCSC Ensembl
Innerchr1:28752493..28753870hg38UCSC Ensembl
Outerchr1:28752456..28753907hg38UCSC Ensembl
chr1:29078986..29080400hg19UCSC Ensembl
Innerchr1:29079005..29080382hg19UCSC Ensembl
Outerchr1:29078968..29080419hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381415
hg191415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9894793
SamplesHG03105
Known GenesYTHDF2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585591
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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