A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697662



Internal ID15063382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11486476..11592874hg38UCSC Ensembl
InnerchrY:11487476..11591874hg38UCSC Ensembl
OuterchrY:11485476..11592902hg38UCSC Ensembl
chrY:13642152..13748550hg19UCSC Ensembl
InnerchrY:13643152..13747550hg19UCSC Ensembl
OuterchrY:13641152..13748578hg19UCSC Ensembl
chrY:12102152..12208550hg18UCSC Ensembl
InnerchrY:12103152..12207550hg18UCSC Ensembl
OuterchrY:12101152..12209550hg18UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg38106399
hg19106399
hg18106399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3383215
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697662
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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