A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101881



Internal ID21291412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:7161666..7169831hg38UCSC Ensembl
InnerchrY:7029707..7037872hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg388166
hg198166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115638
Supporting Variants
Samplessample73
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101881
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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