A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076751



Internal ID19317473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:25362752..25390453hg38UCSC Ensembl
chrY:27508899..27536600hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3827702
hg1927702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770671
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076751
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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