A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6876112



Internal ID9925297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:52857864..52858090hg38UCSC Ensembl
OuterchrX:52886893..52887119hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2740172, esv2740170, esv2740171
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)essv6876112
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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