A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585713



Internal ID6626028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35039239..35041639hg38UCSC Ensembl
Innerchr1:35039239..35041639hg38UCSC Ensembl
Outerchr1:35039063..35041807hg38UCSC Ensembl
chr1:35504840..35507240hg19UCSC Ensembl
Innerchr1:35504840..35507240hg19UCSC Ensembl
Outerchr1:35504664..35507408hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382401
hg192401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9899606, essv9899607
SamplesNA19917, HG00560
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585713
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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