A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116096



Internal ID21299362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21378030..21382658hg38UCSC Ensembl
InnerchrY:23539916..23544544hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg384629
hg194629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102246
Samplessample234
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116096
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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