A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6957838



Internal ID9719740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:24083323..24083768hg38UCSC Ensembl
OuterchrX:24101440..24101885hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2740010, esv2740011
Supporting Variants
SamplesSSM026
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)essv6957838
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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