A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2995368



Internal ID15647897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:22215717..22318915hg38UCSC Ensembl
InnerchrY:24361864..24465062hg19UCSC Ensembl
InnerchrY:22771252..22874450hg18UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38103199
hg19103199
hg18103199
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515226
Supporting Variants
SamplesNA12777
Known GenesLOC100652931, RBMY1F, RBMY2FP, TTTY5
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2995368
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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