A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585762



Internal ID6973283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38069475..38074622hg38UCSC Ensembl
Innerchr1:38069496..38074601hg38UCSC Ensembl
Outerchr1:38069454..38074643hg38UCSC Ensembl
chr1:38535147..38540294hg19UCSC Ensembl
Innerchr1:38535168..38540273hg19UCSC Ensembl
Outerchr1:38535126..38540315hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385148
hg195148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9914489
SamplesHG03565
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585762
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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