A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767832



Internal ID19315343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3977658..3986859hg38UCSC Ensembl
chrY:3845699..3854900hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg389202
hg199202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078151
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767832
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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