A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6690961



Internal ID10104032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:118494740..118495145hg38UCSC Ensembl
OuterchrX:117628703..117629108hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2740422
Supporting Variants
SamplesSSM036
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)essv6690961
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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