A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6892058



Internal ID10286333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56734893..56763381hg38UCSC Ensembl
OuterchrY:58827490..58855978hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3828489
hg1928489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2740708
Supporting Variants
SamplesSSM097
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)essv6892058
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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