A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078705



Internal ID19325133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11261123..11270324hg38UCSC Ensembl
chrY:13416799..13426000hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg389202
hg199202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764494
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078705
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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