A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3429420



Internal ID15276376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21529078..21533376hg38UCSC Ensembl
InnerchrY:21530078..21532376hg38UCSC Ensembl
OuterchrY:21528078..21534376hg38UCSC Ensembl
chrY:23690964..23695262hg19UCSC Ensembl
InnerchrY:23691964..23694262hg19UCSC Ensembl
OuterchrY:23689964..23696262hg19UCSC Ensembl
chrY:22100352..22104650hg18UCSC Ensembl
InnerchrY:22101352..22103650hg18UCSC Ensembl
OuterchrY:22099352..22105650hg18UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg384299
hg194299
hg184299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697670
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3429420
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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