A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6687667



Internal ID10101584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:24274604..24274919hg38UCSC Ensembl
OuterchrX:24292721..24293036hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2740012
Supporting Variants
SamplesSSM035
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)essv6687667
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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