A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6763970



Internal ID10170194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:26658130..26669954hg38UCSC Ensembl
OuterchrY:28804277..28816101hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3811825
hg1911825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2740704, esv2740702
Supporting Variants
SamplesSSM062
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)essv6763970
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