A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768497



Internal ID19315448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3888658..3892659hg38UCSC Ensembl
chrY:3756699..3760700hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg384002
hg194002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078702
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768497
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer