A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102277



Internal ID21282132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:20763414..20764160hg38UCSC Ensembl
InnerchrY:22925300..22926046hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112907
Supporting Variants
Samplessample321
Known GenesRPS4Y2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102277
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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