A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078165



Internal ID19321375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56673271..56771472hg38UCSC Ensembl
chrY:58819399..58917600hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3898202
hg1998202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764015
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078165
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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