A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117292



Internal ID21300558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:22209727..22275365hg38UCSC Ensembl
InnerchrY:24355874..24421512hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3865639
hg1965639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102208
Samplessample125
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117292
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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