A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2740094



Internal ID10323730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:37892630..37893452hg38UCSC Ensembl
OuterchrX:37751883..37752705hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6708852, essv6667829, essv6671873, essv6765219, essv6737328, essv6706732, essv6734684, essv6975688, essv6727612, essv6757715, essv6892232
SamplesSSM059, SSM008, SSM046, SSM050, SSM041, SSM029, SSM031, SSM006, SSM049, SSM030, SSM012
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)esv2740094
Frequency
Sample Size96
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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