A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766646



Internal ID19310901
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 StatusS
Merged Variantsnsv1076306
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766646
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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