A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6856061



Internal ID10253938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:152872589..152872691hg38UCSC Ensembl
OuterchrX:152041133..152041235hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2740622, esv2740621, esv2740620
Supporting Variants
SamplesSSM087
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)essv6856061
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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