A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075763



Internal ID19326837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56829765..56830050hg38UCSC Ensembl
chrY:58975912..58976197hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767640
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075763
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