A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6877385



Internal ID9926442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11533769..11538816hg38UCSC Ensembl
OuterchrY:13689445..13694492hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg385048
hg195048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2740649, esv2740648, esv2740645, esv2740650, esv2740647, esv2740644, esv2740646
Supporting Variants
SamplesSSM092
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6877385
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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