A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6771283



Internal ID10177637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:1603514..1603994hg38UCSC Ensembl
OuterchrX:1722407..1722887hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739743
Supporting Variants
SamplesSSM065
Known GenesASMT
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)essv6771283
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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