A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076306



Internal ID19315860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26648422..26670389hg38UCSC Ensembl
chrY:28794569..28816536hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3821968
hg1921968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766646
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076306
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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