A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101873



Internal ID21289142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:11042694..11550798hg38UCSC Ensembl
InnerchrY:13198370..13706474hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg38508105
hg19508105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116879
Supporting Variants
Samplessample43
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101873
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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