A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585561



Internal ID6973083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27675005..27675859hg38UCSC Ensembl
Innerchr1:27675027..27675838hg38UCSC Ensembl
Outerchr1:27674984..27675881hg38UCSC Ensembl
chr1:28001516..28002370hg19UCSC Ensembl
Innerchr1:28001538..28002349hg19UCSC Ensembl
Outerchr1:28001495..28002392hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9894313, essv9894314, essv9894315
SamplesHG03054, HG03470, HG02051
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585561
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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