A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6671860



Internal ID9739137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:17502523..17502797hg38UCSC Ensembl
OuterchrX:17520646..17520920hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739994, esv2739996
Supporting Variants
SamplesSSM031
Known GenesNHS
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)essv6671860
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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